Name: rs71536199
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs71536199

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:33594334-33594355 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₁ / del(T)₁₀ / del(T)₉ / de…
del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₄ / dup(T)₁₅ / dup(T)₁₇
Variation Type: Indel Insertion and Deletion
Frequency: dup(T)₄=0.1911 (1019/5332, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC00336 : 2KB Upstream Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	5332	TTTTTTTTTTTTTTTTTTTTTT=0.5653	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0730, TTTTTTTTTTTTTTTTTTTTTTTT=0.1017, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0156, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.1911, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0446, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0088, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.767101	0.190554	0.042345	32
European	Sub	4996	TTTTTTTTTTTTTTTTTTTTTT=0.5370	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0777, TTTTTTTTTTTTTTTTTTTTTTTT=0.1083, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0166, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.2034, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0476, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0094, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.74463	0.208831	0.046539	32
African	Sub	272	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	14	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	258	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	8	TTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	30	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	24	TTTTTTTTTTTTTTTTTTTTTT=0.79	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.04, TTTTTTTTTTTTTTTTTTTTTTTT=0.04, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.12, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.9	0.1	0.0	6

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	5332	(T)₂₂=0.5653	del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0730, dupTT=0.1017, dupTTT=0.0156, dup(T)₄=0.1911, dup(T)₅=0.0446, dup(T)₆=0.0000, dup(T)₇=0.0088, dup(T)₈=0.0000, dup(T)₉=0.0000, dup(T)₁₀=0.0000, dup(T)₁₂=0.0000
Allele Frequency Aggregator	European	Sub	4996	(T)₂₂=0.5370	del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0777, dupTT=0.1083, dupTTT=0.0166, dup(T)₄=0.2034, dup(T)₅=0.0476, dup(T)₆=0.0000, dup(T)₇=0.0094, dup(T)₈=0.0000, dup(T)₉=0.0000, dup(T)₁₀=0.0000, dup(T)₁₂=0.0000
Allele Frequency Aggregator	African	Sub	272	(T)₂₂=1.000	del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₀=0.000, dup(T)₁₂=0.000
Allele Frequency Aggregator	Latin American 2	Sub	30	(T)₂₂=1.00	del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00, dup(T)₁₂=0.00
Allele Frequency Aggregator	Other	Sub	24	(T)₂₂=0.79	del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.04, dupTT=0.04, dupTTT=0.00, dup(T)₄=0.12, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00, dup(T)₁₂=0.00
Allele Frequency Aggregator	Latin American 1	Sub	8	(T)₂₂=1.0	del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0, dup(T)₈=0.0, dup(T)₉=0.0, dup(T)₁₀=0.0, dup(T)₁₂=0.0
Allele Frequency Aggregator	South Asian	Sub	2	(T)₂₂=1.0	del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0, dup(T)₈=0.0, dup(T)₉=0.0, dup(T)₁₀=0.0, dup(T)₁₂=0.0
Allele Frequency Aggregator	Asian	Sub	0	(T)₂₂=0	del(T)₁₁=0, del(T)₁₀=0, del(T)₉=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0, dup(T)₆=0, dup(T)₇=0, dup(T)₈=0, dup(T)₉=0, dup(T)₁₀=0, dup(T)₁₂=0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 6	NC_000006.12:g.33594345_33594355del
GRCh38.p14 chr 6	NC_000006.12:g.33594346_33594355del
GRCh38.p14 chr 6	NC_000006.12:g.33594347_33594355del
GRCh38.p14 chr 6	NC_000006.12:g.33594348_33594355del
GRCh38.p14 chr 6	NC_000006.12:g.33594349_33594355del
GRCh38.p14 chr 6	NC_000006.12:g.33594350_33594355del
GRCh38.p14 chr 6	NC_000006.12:g.33594351_33594355del
GRCh38.p14 chr 6	NC_000006.12:g.33594352_33594355del
GRCh38.p14 chr 6	NC_000006.12:g.33594353_33594355del
GRCh38.p14 chr 6	NC_000006.12:g.33594354_33594355del
GRCh38.p14 chr 6	NC_000006.12:g.33594355del
GRCh38.p14 chr 6	NC_000006.12:g.33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594354_33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594353_33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594352_33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594351_33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594350_33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594349_33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594348_33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594347_33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594346_33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594345_33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594344_33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594343_33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594342_33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594341_33594355dup
GRCh38.p14 chr 6	NC_000006.12:g.33594339_33594355dup
GRCh37.p13 chr 6	NC_000006.11:g.33562122_33562132del
GRCh37.p13 chr 6	NC_000006.11:g.33562123_33562132del
GRCh37.p13 chr 6	NC_000006.11:g.33562124_33562132del
GRCh37.p13 chr 6	NC_000006.11:g.33562125_33562132del
GRCh37.p13 chr 6	NC_000006.11:g.33562126_33562132del
GRCh37.p13 chr 6	NC_000006.11:g.33562127_33562132del
GRCh37.p13 chr 6	NC_000006.11:g.33562128_33562132del
GRCh37.p13 chr 6	NC_000006.11:g.33562129_33562132del
GRCh37.p13 chr 6	NC_000006.11:g.33562130_33562132del
GRCh37.p13 chr 6	NC_000006.11:g.33562131_33562132del
GRCh37.p13 chr 6	NC_000006.11:g.33562132del
GRCh37.p13 chr 6	NC_000006.11:g.33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562131_33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562130_33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562129_33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562128_33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562127_33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562126_33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562125_33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562124_33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562123_33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562122_33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562121_33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562120_33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562119_33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562118_33562132dup
GRCh37.p13 chr 6	NC_000006.11:g.33562116_33562132dup

Gene: LINC00336, long intergenic non-protein coding RNA 336 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LINC00336 transcript	NR_027908.2:n.	N/A	Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₂=	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₄	dup(T)₁₅	dup(T)₁₇
GRCh38.p14 chr 6	NC_000006.12:g.33594334_33594355=	NC_000006.12:g.33594345_33594355del	NC_000006.12:g.33594346_33594355del	NC_000006.12:g.33594347_33594355del	NC_000006.12:g.33594348_33594355del	NC_000006.12:g.33594349_33594355del	NC_000006.12:g.33594350_33594355del	NC_000006.12:g.33594351_33594355del	NC_000006.12:g.33594352_33594355del	NC_000006.12:g.33594353_33594355del	NC_000006.12:g.33594354_33594355del	NC_000006.12:g.33594355del	NC_000006.12:g.33594355dup	NC_000006.12:g.33594354_33594355dup	NC_000006.12:g.33594353_33594355dup	NC_000006.12:g.33594352_33594355dup	NC_000006.12:g.33594351_33594355dup	NC_000006.12:g.33594350_33594355dup	NC_000006.12:g.33594349_33594355dup	NC_000006.12:g.33594348_33594355dup	NC_000006.12:g.33594347_33594355dup	NC_000006.12:g.33594346_33594355dup	NC_000006.12:g.33594345_33594355dup	NC_000006.12:g.33594344_33594355dup	NC_000006.12:g.33594343_33594355dup	NC_000006.12:g.33594342_33594355dup	NC_000006.12:g.33594341_33594355dup	NC_000006.12:g.33594339_33594355dup
GRCh37.p13 chr 6	NC_000006.11:g.33562111_33562132=	NC_000006.11:g.33562122_33562132del	NC_000006.11:g.33562123_33562132del	NC_000006.11:g.33562124_33562132del	NC_000006.11:g.33562125_33562132del	NC_000006.11:g.33562126_33562132del	NC_000006.11:g.33562127_33562132del	NC_000006.11:g.33562128_33562132del	NC_000006.11:g.33562129_33562132del	NC_000006.11:g.33562130_33562132del	NC_000006.11:g.33562131_33562132del	NC_000006.11:g.33562132del	NC_000006.11:g.33562132dup	NC_000006.11:g.33562131_33562132dup	NC_000006.11:g.33562130_33562132dup	NC_000006.11:g.33562129_33562132dup	NC_000006.11:g.33562128_33562132dup	NC_000006.11:g.33562127_33562132dup	NC_000006.11:g.33562126_33562132dup	NC_000006.11:g.33562125_33562132dup	NC_000006.11:g.33562124_33562132dup	NC_000006.11:g.33562123_33562132dup	NC_000006.11:g.33562122_33562132dup	NC_000006.11:g.33562121_33562132dup	NC_000006.11:g.33562120_33562132dup	NC_000006.11:g.33562119_33562132dup	NC_000006.11:g.33562118_33562132dup	NC_000006.11:g.33562116_33562132dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

57 SubSNP, 38 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss98453258	Feb 13, 2009 (130)
2	PJP	ss295274278	Oct 12, 2018 (152)
3	PJP	ss295274279	Oct 12, 2018 (152)
4	SWEGEN	ss2998858047	Nov 08, 2017 (151)
5	SWEGEN	ss2998858048	Nov 08, 2017 (151)
6	SWEGEN	ss2998858049	Nov 08, 2017 (151)
7	SWEGEN	ss2998858050	Nov 08, 2017 (151)
8	SWEGEN	ss2998858051	Nov 08, 2017 (151)
9	EVA_DECODE	ss3716958158	Jul 13, 2019 (153)
10	EVA_DECODE	ss3716958159	Jul 13, 2019 (153)
11	EVA_DECODE	ss3716958160	Jul 13, 2019 (153)
12	EVA_DECODE	ss3716958161	Jul 13, 2019 (153)
13	PACBIO	ss3785440296	Jul 13, 2019 (153)
14	PACBIO	ss3790797083	Jul 13, 2019 (153)
15	PACBIO	ss3790797084	Jul 13, 2019 (153)
16	PACBIO	ss3795675686	Jul 13, 2019 (153)
17	PACBIO	ss3795675687	Jul 13, 2019 (153)
18	EVA	ss3829858294	Apr 26, 2020 (154)
19	GNOMAD	ss4139602358	Apr 26, 2021 (155)
20	GNOMAD	ss4139602361	Apr 26, 2021 (155)
21	GNOMAD	ss4139602362	Apr 26, 2021 (155)
22	GNOMAD	ss4139602363	Apr 26, 2021 (155)
23	GNOMAD	ss4139602364	Apr 26, 2021 (155)
24	GNOMAD	ss4139602365	Apr 26, 2021 (155)
25	GNOMAD	ss4139602366	Apr 26, 2021 (155)
26	GNOMAD	ss4139602367	Apr 26, 2021 (155)
27	GNOMAD	ss4139602368	Apr 26, 2021 (155)
28	GNOMAD	ss4139602369	Apr 26, 2021 (155)
29	GNOMAD	ss4139602370	Apr 26, 2021 (155)
30	GNOMAD	ss4139602371	Apr 26, 2021 (155)
31	GNOMAD	ss4139602372	Apr 26, 2021 (155)
32	GNOMAD	ss4139602373	Apr 26, 2021 (155)
33	GNOMAD	ss4139602374	Apr 26, 2021 (155)
34	GNOMAD	ss4139602375	Apr 26, 2021 (155)
35	GNOMAD	ss4139602377	Apr 26, 2021 (155)
36	GNOMAD	ss4139602378	Apr 26, 2021 (155)
37	GNOMAD	ss4139602379	Apr 26, 2021 (155)
38	GNOMAD	ss4139602380	Apr 26, 2021 (155)
39	GNOMAD	ss4139602381	Apr 26, 2021 (155)
40	GNOMAD	ss4139602382	Apr 26, 2021 (155)
41	GNOMAD	ss4139602383	Apr 26, 2021 (155)
42	GNOMAD	ss4139602384	Apr 26, 2021 (155)
43	GNOMAD	ss4139602385	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5176944053	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5176944054	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5176944055	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5176944056	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5176944057	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5176944058	Apr 26, 2021 (155)
50	HUGCELL_USP	ss5465717242	Oct 17, 2022 (156)
51	HUGCELL_USP	ss5465717243	Oct 17, 2022 (156)
52	TOMMO_GENOMICS	ss5714824346	Oct 17, 2022 (156)
53	TOMMO_GENOMICS	ss5714824347	Oct 17, 2022 (156)
54	TOMMO_GENOMICS	ss5714824348	Oct 17, 2022 (156)
55	TOMMO_GENOMICS	ss5714824349	Oct 17, 2022 (156)
56	TOMMO_GENOMICS	ss5714824350	Oct 17, 2022 (156)
57	EVA	ss5855303264	Oct 17, 2022 (156)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221606249 (NC_000006.12:33594333::T 15021/60644) Row 221606252 (NC_000006.12:33594333::TT 9584/61044) Row 221606253 (NC_000006.12:33594333::TTT 503/61358)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 34913360 (NC_000006.11:33562110::T 6507/15896) Row 34913361 (NC_000006.11:33562110::TTT 136/15896) Row 34913362 (NC_000006.11:33562110::TTTT 3120/15896)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 34913360 (NC_000006.11:33562110::T 6507/15896) Row 34913361 (NC_000006.11:33562110::TTT 136/15896) Row 34913362 (NC_000006.11:33562110::TTTT 3120/15896)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 34913360 (NC_000006.11:33562110::T 6507/15896) Row 34913361 (NC_000006.11:33562110::TTT 136/15896) Row 34913362 (NC_000006.11:33562110::TTTT 3120/15896)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 34913360 (NC_000006.11:33562110::T 6507/15896) Row 34913361 (NC_000006.11:33562110::TTT 136/15896) Row 34913362 (NC_000006.11:33562110::TTTT 3120/15896)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 34913360 (NC_000006.11:33562110::T 6507/15896) Row 34913361 (NC_000006.11:33562110::TTT 136/15896) Row 34913362 (NC_000006.11:33562110::TTTT 3120/15896)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 34913360 (NC_000006.11:33562110::T 6507/15896) Row 34913361 (NC_000006.11:33562110::TTT 136/15896) Row 34913362 (NC_000006.11:33562110::TTTT 3120/15896)...	-	Apr 26, 2021 (155)
90	14KJPN Submission ignored due to conflicting rows: Row 48661450 (NC_000006.12:33594333::T 11084/25010) Row 48661451 (NC_000006.12:33594333::TTTT 4562/25010) Row 48661452 (NC_000006.12:33594333::TTT 67/25010)...	-	Oct 17, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 48661450 (NC_000006.12:33594333::T 11084/25010) Row 48661451 (NC_000006.12:33594333::TTTT 4562/25010) Row 48661452 (NC_000006.12:33594333::TTT 67/25010)...	-	Oct 17, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 48661450 (NC_000006.12:33594333::T 11084/25010) Row 48661451 (NC_000006.12:33594333::TTTT 4562/25010) Row 48661452 (NC_000006.12:33594333::TTT 67/25010)...	-	Oct 17, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 48661450 (NC_000006.12:33594333::T 11084/25010) Row 48661451 (NC_000006.12:33594333::TTTT 4562/25010) Row 48661452 (NC_000006.12:33594333::TTT 67/25010)...	-	Oct 17, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 48661450 (NC_000006.12:33594333::T 11084/25010) Row 48661451 (NC_000006.12:33594333::TTTT 4562/25010) Row 48661452 (NC_000006.12:33594333::TTT 67/25010)...	-	Oct 17, 2022 (156)
95	ALFA	NC_000006.12 - 33594334	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4139602385	NC_000006.12:33594333:TTTTTTTTTTT:	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4139602384	NC_000006.12:33594333:TTTTTTTTTT:	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4139602383	NC_000006.12:33594333:TTTTTTTTT:	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4139602382	NC_000006.12:33594333:TTTTTTTT:	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4139602381	NC_000006.12:33594333:TTTTTTT:	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4139602380	NC_000006.12:33594333:TTTTT:	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4139602379	NC_000006.12:33594333:TTTT:	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4139602378	NC_000006.12:33594333:TTT:	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4139602377	NC_000006.12:33594333:TT:	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5465717243	NC_000006.12:33594333:T:	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss2998858047, ss3790797083, ss3795675686, ss5176944053	NC_000006.11:33562110::T	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3716958158, ss4139602358, ss5465717242, ss5714824346	NC_000006.12:33594333::T	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss295274278	NC_000006.10:33670089::TT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss295274279	NC_000006.10:33670109::TT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss2998858048, ss3829858294, ss5176944056	NC_000006.11:33562110::TT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3716958159, ss4139602361, ss5714824349	NC_000006.12:33594333::TT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss98453258	NT_007592.15:33502110::TT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss2998858051, ss3785440296, ss3790797084, ss3795675687, ss5176944054	NC_000006.11:33562110::TTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3716958160, ss4139602362, ss5714824348, ss5855303264	NC_000006.12:33594333::TTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss2998858050, ss5176944055	NC_000006.11:33562110::TTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3716958161, ss4139602363, ss5714824347	NC_000006.12:33594333::TTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss2998858049, ss5176944058	NC_000006.11:33562110::TTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139602364, ss5714824350	NC_000006.12:33594333::TTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5176944057	NC_000006.11:33562110::TTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139602365	NC_000006.12:33594333::TTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139602366	NC_000006.12:33594333::TTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139602367	NC_000006.12:33594333::TTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139602368	NC_000006.12:33594333::TTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139602369	NC_000006.12:33594333::TTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139602370	NC_000006.12:33594333::TTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139602371	NC_000006.12:33594333::TTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4905925384	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139602372	NC_000006.12:33594333::TTTTTTTTTTT… NC_000006.12:33594333::TTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139602373	NC_000006.12:33594333::TTTTTTTTTTT… NC_000006.12:33594333::TTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139602374	NC_000006.12:33594333::TTTTTTTTTTT… NC_000006.12:33594333::TTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139602375	NC_000006.12:33594333::TTTTTTTTTTT… NC_000006.12:33594333::TTTTTTTTTTTTTTTTT	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3494207833	NC_000006.12:33594333:TTTTTT:	NC_000006.12:33594333:TTTTTTTTTTTT… NC_000006.12:33594333:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs71536199

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs71536199