Name: rs34213399
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.

rs34213399

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:47864871-47864890 (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)₁₂ / del(T)₁₀ / del(T)₉ / de…
del(T)₁₂ / 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
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₂=0.000004 (1/264690, TOPMED)
(T)₂₀=0.4236 (2058/4858, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC01595 : Intron 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	4858	TTTTTTTTTTTTTTTTTTTT=0.4236	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.5605, TTTTTTTTTTTTTTTTTTTTTT=0.0121, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0006, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0010, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0016, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0004, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.370934	0.505703	0.123363	32
European	Sub	4784	TTTTTTTTTTTTTTTTTTTT=0.4151	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.5688, TTTTTTTTTTTTTTTTTTTTTT=0.0123, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0006, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0010, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0017, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0004, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.361373	0.513305	0.125322	32
African	Sub	46	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
African American	Sub	46	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	4	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
South Asian	Sub	2	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	22	TTTTTTTTTTTTTTTTTTTT=0.91	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.09, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.909091	0.090909	0.0	7

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
TopMed	Global	Study-wide	264690	(T)₂₀=0.999996	del(T)₁₂=0.000004
Allele Frequency Aggregator	Total	Global	4858	(T)₂₀=0.4236	del(T)₁₂=0.0000, del(T)₁₀=0.0000, del(T)₈=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=0.5605, dupTT=0.0121, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0016, dup(T)₆=0.0000, dup(T)₇=0.0004, dup(T)₈=0.0006, dup(T)₁₀=0.0010
Allele Frequency Aggregator	European	Sub	4784	(T)₂₀=0.4151	del(T)₁₂=0.0000, del(T)₁₀=0.0000, del(T)₈=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=0.5688, dupTT=0.0123, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0017, dup(T)₆=0.0000, dup(T)₇=0.0004, dup(T)₈=0.0006, dup(T)₁₀=0.0010
Allele Frequency Aggregator	African	Sub	46	(T)₂₀=1.00	del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₈=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)₁₀=0.00
Allele Frequency Aggregator	Other	Sub	22	(T)₂₀=0.91	del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₈=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=0.09, 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)₁₀=0.00
Allele Frequency Aggregator	Latin American 1	Sub	4	(T)₂₀=1.0	del(T)₁₂=0.0, del(T)₁₀=0.0, del(T)₈=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)₁₀=0.0
Allele Frequency Aggregator	South Asian	Sub	2	(T)₂₀=1.0	del(T)₁₂=0.0, del(T)₁₀=0.0, del(T)₈=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)₁₀=0.0
Allele Frequency Aggregator	Latin American 2	Sub	0	(T)₂₀=0	del(T)₁₂=0, del(T)₁₀=0, del(T)₈=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)₁₀=0
Allele Frequency Aggregator	Asian	Sub	0	(T)₂₀=0	del(T)₁₂=0, del(T)₁₀=0, del(T)₈=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)₁₀=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 19	NC_000019.10:g.47864879_47864890del
GRCh38.p14 chr 19	NC_000019.10:g.47864881_47864890del
GRCh38.p14 chr 19	NC_000019.10:g.47864882_47864890del
GRCh38.p14 chr 19	NC_000019.10:g.47864883_47864890del
GRCh38.p14 chr 19	NC_000019.10:g.47864884_47864890del
GRCh38.p14 chr 19	NC_000019.10:g.47864885_47864890del
GRCh38.p14 chr 19	NC_000019.10:g.47864886_47864890del
GRCh38.p14 chr 19	NC_000019.10:g.47864887_47864890del
GRCh38.p14 chr 19	NC_000019.10:g.47864888_47864890del
GRCh38.p14 chr 19	NC_000019.10:g.47864889_47864890del
GRCh38.p14 chr 19	NC_000019.10:g.47864890del
GRCh38.p14 chr 19	NC_000019.10:g.47864890dup
GRCh38.p14 chr 19	NC_000019.10:g.47864889_47864890dup
GRCh38.p14 chr 19	NC_000019.10:g.47864888_47864890dup
GRCh38.p14 chr 19	NC_000019.10:g.47864887_47864890dup
GRCh38.p14 chr 19	NC_000019.10:g.47864886_47864890dup
GRCh38.p14 chr 19	NC_000019.10:g.47864885_47864890dup
GRCh38.p14 chr 19	NC_000019.10:g.47864884_47864890dup
GRCh38.p14 chr 19	NC_000019.10:g.47864883_47864890dup
GRCh38.p14 chr 19	NC_000019.10:g.47864882_47864890dup
GRCh38.p14 chr 19	NC_000019.10:g.47864881_47864890dup
GRCh37.p13 chr 19	NC_000019.9:g.48368136_48368147del
GRCh37.p13 chr 19	NC_000019.9:g.48368138_48368147del
GRCh37.p13 chr 19	NC_000019.9:g.48368139_48368147del
GRCh37.p13 chr 19	NC_000019.9:g.48368140_48368147del
GRCh37.p13 chr 19	NC_000019.9:g.48368141_48368147del
GRCh37.p13 chr 19	NC_000019.9:g.48368142_48368147del
GRCh37.p13 chr 19	NC_000019.9:g.48368143_48368147del
GRCh37.p13 chr 19	NC_000019.9:g.48368144_48368147del
GRCh37.p13 chr 19	NC_000019.9:g.48368145_48368147del
GRCh37.p13 chr 19	NC_000019.9:g.48368146_48368147del
GRCh37.p13 chr 19	NC_000019.9:g.48368147del
GRCh37.p13 chr 19	NC_000019.9:g.48368147dup
GRCh37.p13 chr 19	NC_000019.9:g.48368146_48368147dup
GRCh37.p13 chr 19	NC_000019.9:g.48368145_48368147dup
GRCh37.p13 chr 19	NC_000019.9:g.48368144_48368147dup
GRCh37.p13 chr 19	NC_000019.9:g.48368143_48368147dup
GRCh37.p13 chr 19	NC_000019.9:g.48368142_48368147dup
GRCh37.p13 chr 19	NC_000019.9:g.48368141_48368147dup
GRCh37.p13 chr 19	NC_000019.9:g.48368140_48368147dup
GRCh37.p13 chr 19	NC_000019.9:g.48368139_48368147dup
GRCh37.p13 chr 19	NC_000019.9:g.48368138_48368147dup

Gene: LINC01595, uncharacterized LINC01595 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC01595 transcript variant X1	XR_936005.3:n.	N/A	Intron Variant
LINC01595 transcript variant X2	XR_936006.3:n.	N/A	Intron 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)₂₀=	del(T)₁₂	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
GRCh38.p14 chr 19	NC_000019.10:g.47864871_47864890=	NC_000019.10:g.47864879_47864890del	NC_000019.10:g.47864881_47864890del	NC_000019.10:g.47864882_47864890del	NC_000019.10:g.47864883_47864890del	NC_000019.10:g.47864884_47864890del	NC_000019.10:g.47864885_47864890del	NC_000019.10:g.47864886_47864890del	NC_000019.10:g.47864887_47864890del	NC_000019.10:g.47864888_47864890del	NC_000019.10:g.47864889_47864890del	NC_000019.10:g.47864890del	NC_000019.10:g.47864890dup	NC_000019.10:g.47864889_47864890dup	NC_000019.10:g.47864888_47864890dup	NC_000019.10:g.47864887_47864890dup	NC_000019.10:g.47864886_47864890dup	NC_000019.10:g.47864885_47864890dup	NC_000019.10:g.47864884_47864890dup	NC_000019.10:g.47864883_47864890dup	NC_000019.10:g.47864882_47864890dup	NC_000019.10:g.47864881_47864890dup
GRCh37.p13 chr 19	NC_000019.9:g.48368128_48368147=	NC_000019.9:g.48368136_48368147del	NC_000019.9:g.48368138_48368147del	NC_000019.9:g.48368139_48368147del	NC_000019.9:g.48368140_48368147del	NC_000019.9:g.48368141_48368147del	NC_000019.9:g.48368142_48368147del	NC_000019.9:g.48368143_48368147del	NC_000019.9:g.48368144_48368147del	NC_000019.9:g.48368145_48368147del	NC_000019.9:g.48368146_48368147del	NC_000019.9:g.48368147del	NC_000019.9:g.48368147dup	NC_000019.9:g.48368146_48368147dup	NC_000019.9:g.48368145_48368147dup	NC_000019.9:g.48368144_48368147dup	NC_000019.9:g.48368143_48368147dup	NC_000019.9:g.48368142_48368147dup	NC_000019.9:g.48368141_48368147dup	NC_000019.9:g.48368140_48368147dup	NC_000019.9:g.48368139_48368147dup	NC_000019.9:g.48368138_48368147dup

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#.

48 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40976956	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss95730591	Feb 13, 2009 (130)
3	PJP	ss294965444	May 09, 2011 (137)
4	PJP	ss294965445	May 09, 2011 (135)
5	SWEGEN	ss3017580327	Nov 08, 2017 (151)
6	SWEGEN	ss3017580328	Nov 08, 2017 (151)
7	EVA_DECODE	ss3702892829	Jul 13, 2019 (153)
8	EVA_DECODE	ss3702892830	Jul 13, 2019 (153)
9	EVA_DECODE	ss3702892831	Jul 13, 2019 (153)
10	EVA_DECODE	ss3702892832	Jul 13, 2019 (153)
11	EVA	ss3835492946	Apr 27, 2020 (154)
12	GNOMAD	ss4332341268	Apr 26, 2021 (155)
13	GNOMAD	ss4332341269	Apr 26, 2021 (155)
14	GNOMAD	ss4332341270	Apr 26, 2021 (155)
15	GNOMAD	ss4332341271	Apr 26, 2021 (155)
16	GNOMAD	ss4332341272	Apr 26, 2021 (155)
17	GNOMAD	ss4332341273	Apr 26, 2021 (155)
18	GNOMAD	ss4332341274	Apr 26, 2021 (155)
19	GNOMAD	ss4332341275	Apr 26, 2021 (155)
20	GNOMAD	ss4332341276	Apr 26, 2021 (155)
21	GNOMAD	ss4332341277	Apr 26, 2021 (155)
22	GNOMAD	ss4332341279	Apr 26, 2021 (155)
23	GNOMAD	ss4332341280	Apr 26, 2021 (155)
24	GNOMAD	ss4332341281	Apr 26, 2021 (155)
25	GNOMAD	ss4332341282	Apr 26, 2021 (155)
26	GNOMAD	ss4332341283	Apr 26, 2021 (155)
27	GNOMAD	ss4332341284	Apr 26, 2021 (155)
28	GNOMAD	ss4332341285	Apr 26, 2021 (155)
29	GNOMAD	ss4332341286	Apr 26, 2021 (155)
30	GNOMAD	ss4332341287	Apr 26, 2021 (155)
31	TOPMED	ss5076934552	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5228063229	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5228063230	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5228063231	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5228063232	Apr 26, 2021 (155)
36	1000G_HIGH_COVERAGE	ss5307481861	Oct 13, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5307481862	Oct 13, 2022 (156)
38	HUGCELL_USP	ss5499965348	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5499965349	Oct 13, 2022 (156)
40	HUGCELL_USP	ss5499965350	Oct 13, 2022 (156)
41	TOMMO_GENOMICS	ss5786798395	Oct 13, 2022 (156)
42	TOMMO_GENOMICS	ss5786798396	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5786798398	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5786798399	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5786798400	Oct 13, 2022 (156)
46	EVA	ss5840638499	Oct 13, 2022 (156)
47	EVA	ss5840638500	Oct 13, 2022 (156)
48	EVA	ss5840638501	Oct 13, 2022 (156)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541865826 (NC_000019.10:47864870::T 62658/80630) Row 541865827 (NC_000019.10:47864870::TT 1575/80396) Row 541865828 (NC_000019.10:47864870::TTT 33/80650)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 86032536 (NC_000019.9:48368127::T 13184/15840) Row 86032537 (NC_000019.9:48368127::TTTTT 120/15840) Row 86032538 (NC_000019.9:48368127::TT 49/15840)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 86032536 (NC_000019.9:48368127::T 13184/15840) Row 86032537 (NC_000019.9:48368127::TTTTT 120/15840) Row 86032538 (NC_000019.9:48368127::TT 49/15840)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 86032536 (NC_000019.9:48368127::T 13184/15840) Row 86032537 (NC_000019.9:48368127::TTTTT 120/15840) Row 86032538 (NC_000019.9:48368127::TT 49/15840)...	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 86032536 (NC_000019.9:48368127::T 13184/15840) Row 86032537 (NC_000019.9:48368127::TTTTT 120/15840) Row 86032538 (NC_000019.9:48368127::TT 49/15840)...	-	Apr 26, 2021 (155)
72	14KJPN Submission ignored due to conflicting rows: Row 120635499 (NC_000019.10:47864870::T 20532/25434) Row 120635500 (NC_000019.10:47864870::TTTTT 170/25434) Row 120635502 (NC_000019.10:47864870::TT 70/25434)...	-	Oct 13, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 120635499 (NC_000019.10:47864870::T 20532/25434) Row 120635500 (NC_000019.10:47864870::TTTTT 170/25434) Row 120635502 (NC_000019.10:47864870::TT 70/25434)...	-	Oct 13, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 120635499 (NC_000019.10:47864870::T 20532/25434) Row 120635500 (NC_000019.10:47864870::TTTTT 170/25434) Row 120635502 (NC_000019.10:47864870::TT 70/25434)...	-	Oct 13, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 120635499 (NC_000019.10:47864870::T 20532/25434) Row 120635500 (NC_000019.10:47864870::TTTTT 170/25434) Row 120635502 (NC_000019.10:47864870::TT 70/25434)...	-	Oct 13, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 120635499 (NC_000019.10:47864870::T 20532/25434) Row 120635500 (NC_000019.10:47864870::TTTTT 170/25434) Row 120635502 (NC_000019.10:47864870::TT 70/25434)...	-	Oct 13, 2022 (156)
77	TopMed	NC_000019.10 - 47864871	Apr 26, 2021 (155)
78	ALFA	NC_000019.10 - 47864871	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).

Associated ID	History Updated (Build)
rs72044060	May 11, 2012 (137)
rs145356327	Sep 17, 2011 (135)
rs147655821	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
292480216, ss5076934552	NC_000019.10:47864870:TTTTTTTTTTTT:	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss4332341287	NC_000019.10:47864870:TTTTTTTTTT:	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4332341286	NC_000019.10:47864870:TTTTTTTTT:	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4332341285	NC_000019.10:47864870:TTTTTTT:	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4332341284	NC_000019.10:47864870:TTTTTT:	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4332341283	NC_000019.10:47864870:TTTTT:	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4332341282	NC_000019.10:47864870:TTTT:	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4332341281	NC_000019.10:47864870:TTT:	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3702892829, ss4332341280	NC_000019.10:47864870:TT:	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4332341279, ss5307481862, ss5499965348, ss5786798400	NC_000019.10:47864870:T:	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3702892830	NC_000019.10:47864871:T:	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss294965444	NC_000019.8:53059940::T	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss294965445	NC_000019.8:53059959::T	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3017580327, ss3835492946, ss5228063229, ss5840638499	NC_000019.9:48368127::T	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4332341268, ss5307481861, ss5499965349, ss5786798395	NC_000019.10:47864870::T	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3702892831	NC_000019.10:47864872::T	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss40976956	NT_011109.16:20636345::T	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss95730591	NT_011109.16:20636365::T	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3017580328, ss5228063231, ss5840638500	NC_000019.9:48368127::TT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332341269, ss5499965350, ss5786798398	NC_000019.10:47864870::TT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3702892832	NC_000019.10:47864872::TT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5840638501	NC_000019.9:48368127::TTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT
ss4332341270	NC_000019.10:47864870::TTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5228063232	NC_000019.9:48368127::TTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332341271, ss5786798399	NC_000019.10:47864870::TTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5228063230	NC_000019.9:48368127::TTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332341272, ss5786798396	NC_000019.10:47864870::TTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332341273	NC_000019.10:47864870::TTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332341274	NC_000019.10:47864870::TTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332341275	NC_000019.10:47864870::TTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332341276	NC_000019.10:47864870::TTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332341277	NC_000019.10:47864870::TTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9537876989	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:47864870:TTTTTTTTTTTT… NC_000019.10:47864870:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs34213399

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs34213399