Name: rs71171183
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.

rs71171183

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr18:67508732-67508747 (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)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₅
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.2887 (1781/6168, ALFA)
dupT=0.3329 (1667/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DSEL : 3 Prime UTR 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	6168	TTTTTTTTTTTTTTTT=0.6349	TTTTT=0.0000, TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0058, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.2887, TTTTTTTTTTTTTTTTTT=0.0670, TTTTTTTTTTTTTTTTTTT=0.0019, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0011, TTTTTTTTTTTTTTTTTTTT=0.0000	0.631715	0.220452	0.147833	32
European	Sub	5508	TTTTTTTTTTTTTTTT=0.5922	TTTTT=0.0000, TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0065, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.3223, TTTTTTTTTTTTTTTTTT=0.0750, TTTTTTTTTTTTTTTTTTT=0.0022, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0013, TTTTTTTTTTTTTTTTTTTT=0.0000	0.58168	0.249894	0.168425	32
African	Sub	436	TTTTTTTTTTTTTTTT=1.000	TTTTT=0.000, TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	14	TTTTTTTTTTTTTTTT=1.00	TTTTT=0.00, TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	422	TTTTTTTTTTTTTTTT=1.000	TTTTT=0.000, TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	4	TTTTTTTTTTTTTTTT=1.0	TTTTT=0.0, TTTTTT=0.0, TTTTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTT=0	TTTTT=0, TTTTTT=0, TTTTTTT=0, TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTT=1.0	TTTTT=0.0, TTTTTT=0.0, TTTTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	20	TTTTTTTTTTTTTTTT=1.00	TTTTT=0.00, TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	118	TTTTTTTTTTTTTTTT=1.000	TTTTT=0.000, TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	14	TTTTTTTTTTTTTTTT=1.00	TTTTT=0.00, TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	68	TTTTTTTTTTTTTTTT=0.91	TTTTT=0.00, TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.09, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	0.911765	0.088235	0.0	19

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	6168	(T)₁₆=0.6349	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=0.0058, delTT=0.0000, delT=0.0000, dupT=0.2887, dupTT=0.0670, dupTTT=0.0019, dup(T)₄=0.0000, dup(T)₉=0.0011, dup(T)₁₅=0.0005
Allele Frequency Aggregator	European	Sub	5508	(T)₁₆=0.5922	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=0.0065, delTT=0.0000, delT=0.0000, dupT=0.3223, dupTT=0.0750, dupTTT=0.0022, dup(T)₄=0.0000, dup(T)₉=0.0013, dup(T)₁₅=0.0005
Allele Frequency Aggregator	African	Sub	436	(T)₁₆=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)₉=0.000, dup(T)₁₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	118	(T)₁₆=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)₉=0.000, dup(T)₁₅=0.000
Allele Frequency Aggregator	Other	Sub	68	(T)₁₆=0.91	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=0.09, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₉=0.00, dup(T)₁₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	20	(T)₁₆=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)₉=0.00, dup(T)₁₅=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(T)₁₆=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)₉=0.00, dup(T)₁₅=0.00
Allele Frequency Aggregator	Asian	Sub	4	(T)₁₆=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)₉=0.0, dup(T)₁₅=0.0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.3329
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.3011
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.3512
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.3638
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.338
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.314

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 18	NC_000018.10:g.67508737_67508747del
GRCh38.p14 chr 18	NC_000018.10:g.67508738_67508747del
GRCh38.p14 chr 18	NC_000018.10:g.67508739_67508747del
GRCh38.p14 chr 18	NC_000018.10:g.67508740_67508747del
GRCh38.p14 chr 18	NC_000018.10:g.67508741_67508747del
GRCh38.p14 chr 18	NC_000018.10:g.67508742_67508747del
GRCh38.p14 chr 18	NC_000018.10:g.67508743_67508747del
GRCh38.p14 chr 18	NC_000018.10:g.67508744_67508747del
GRCh38.p14 chr 18	NC_000018.10:g.67508745_67508747del
GRCh38.p14 chr 18	NC_000018.10:g.67508746_67508747del
GRCh38.p14 chr 18	NC_000018.10:g.67508747del
GRCh38.p14 chr 18	NC_000018.10:g.67508747dup
GRCh38.p14 chr 18	NC_000018.10:g.67508746_67508747dup
GRCh38.p14 chr 18	NC_000018.10:g.67508745_67508747dup
GRCh38.p14 chr 18	NC_000018.10:g.67508744_67508747dup
GRCh38.p14 chr 18	NC_000018.10:g.67508740_67508747dup
GRCh38.p14 chr 18	NC_000018.10:g.67508739_67508747dup
GRCh38.p14 chr 18	NC_000018.10:g.67508738_67508747dup
GRCh38.p14 chr 18	NC_000018.10:g.67508733_67508747dup
GRCh37.p13 chr 18	NC_000018.9:g.65175974_65175984del
GRCh37.p13 chr 18	NC_000018.9:g.65175975_65175984del
GRCh37.p13 chr 18	NC_000018.9:g.65175976_65175984del
GRCh37.p13 chr 18	NC_000018.9:g.65175977_65175984del
GRCh37.p13 chr 18	NC_000018.9:g.65175978_65175984del
GRCh37.p13 chr 18	NC_000018.9:g.65175979_65175984del
GRCh37.p13 chr 18	NC_000018.9:g.65175980_65175984del
GRCh37.p13 chr 18	NC_000018.9:g.65175981_65175984del
GRCh37.p13 chr 18	NC_000018.9:g.65175982_65175984del
GRCh37.p13 chr 18	NC_000018.9:g.65175983_65175984del
GRCh37.p13 chr 18	NC_000018.9:g.65175984del
GRCh37.p13 chr 18	NC_000018.9:g.65175984dup
GRCh37.p13 chr 18	NC_000018.9:g.65175983_65175984dup
GRCh37.p13 chr 18	NC_000018.9:g.65175982_65175984dup
GRCh37.p13 chr 18	NC_000018.9:g.65175981_65175984dup
GRCh37.p13 chr 18	NC_000018.9:g.65175977_65175984dup
GRCh37.p13 chr 18	NC_000018.9:g.65175976_65175984dup
GRCh37.p13 chr 18	NC_000018.9:g.65175975_65175984dup
GRCh37.p13 chr 18	NC_000018.9:g.65175970_65175984dup
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154464_154474del
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154465_154474del
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154466_154474del
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154467_154474del
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154468_154474del
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154469_154474del
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154470_154474del
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154471_154474del
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154472_154474del
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154473_154474del
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154474del
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154474dup
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154473_154474dup
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154472_154474dup
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154471_154474dup
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154467_154474dup
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154466_154474dup
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154465_154474dup
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154460_154474dup

Gene: DSEL, dermatan sulfate epimerase like (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DSEL transcript	NM_032160.3:c.2223_2238=	N/A	3 Prime UTR 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)₁₆=	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)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₅
GRCh38.p14 chr 18	NC_000018.10:g.67508732_67508747=	NC_000018.10:g.67508737_67508747del	NC_000018.10:g.67508738_67508747del	NC_000018.10:g.67508739_67508747del	NC_000018.10:g.67508740_67508747del	NC_000018.10:g.67508741_67508747del	NC_000018.10:g.67508742_67508747del	NC_000018.10:g.67508743_67508747del	NC_000018.10:g.67508744_67508747del	NC_000018.10:g.67508745_67508747del	NC_000018.10:g.67508746_67508747del	NC_000018.10:g.67508747del	NC_000018.10:g.67508747dup	NC_000018.10:g.67508746_67508747dup	NC_000018.10:g.67508745_67508747dup	NC_000018.10:g.67508744_67508747dup	NC_000018.10:g.67508740_67508747dup	NC_000018.10:g.67508739_67508747dup	NC_000018.10:g.67508738_67508747dup	NC_000018.10:g.67508733_67508747dup
GRCh37.p13 chr 18	NC_000018.9:g.65175969_65175984=	NC_000018.9:g.65175974_65175984del	NC_000018.9:g.65175975_65175984del	NC_000018.9:g.65175976_65175984del	NC_000018.9:g.65175977_65175984del	NC_000018.9:g.65175978_65175984del	NC_000018.9:g.65175979_65175984del	NC_000018.9:g.65175980_65175984del	NC_000018.9:g.65175981_65175984del	NC_000018.9:g.65175982_65175984del	NC_000018.9:g.65175983_65175984del	NC_000018.9:g.65175984del	NC_000018.9:g.65175984dup	NC_000018.9:g.65175983_65175984dup	NC_000018.9:g.65175982_65175984dup	NC_000018.9:g.65175981_65175984dup	NC_000018.9:g.65175977_65175984dup	NC_000018.9:g.65175976_65175984dup	NC_000018.9:g.65175975_65175984dup	NC_000018.9:g.65175970_65175984dup
GRCh38.p14 chr 18 alt locus HSCHR18_2_CTG2	NW_003315960.1:g.154459_154474=	NW_003315960.1:g.154464_154474del	NW_003315960.1:g.154465_154474del	NW_003315960.1:g.154466_154474del	NW_003315960.1:g.154467_154474del	NW_003315960.1:g.154468_154474del	NW_003315960.1:g.154469_154474del	NW_003315960.1:g.154470_154474del	NW_003315960.1:g.154471_154474del	NW_003315960.1:g.154472_154474del	NW_003315960.1:g.154473_154474del	NW_003315960.1:g.154474del	NW_003315960.1:g.154474dup	NW_003315960.1:g.154473_154474dup	NW_003315960.1:g.154472_154474dup	NW_003315960.1:g.154471_154474dup	NW_003315960.1:g.154467_154474dup	NW_003315960.1:g.154466_154474dup	NW_003315960.1:g.154465_154474dup	NW_003315960.1:g.154460_154474dup
DSEL transcript	NM_032160.3:c.2223_2238=	NM_032160.3:c.2228_2238del	NM_032160.3:c.2229_2238del	NM_032160.3:c.2230_2238del	NM_032160.3:c.2231_2238del	NM_032160.3:c.2232_2238del	NM_032160.3:c.2233_2238del	NM_032160.3:c.2234_2238del	NM_032160.3:c.2235_2238del	NM_032160.3:c.2236_2238del	NM_032160.3:c.2237_2238del	NM_032160.3:c.*2238del	NM_032160.3:c.*2238dup	NM_032160.3:c.2237_2238dup	NM_032160.3:c.2236_2238dup	NM_032160.3:c.2235_2238dup	NM_032160.3:c.2231_2238dup	NM_032160.3:c.2230_2238dup	NM_032160.3:c.2229_2238dup	NM_032160.3:c.2224_2238dup
DSEL transcript	NM_032160.2:c.2223_2238=	NM_032160.2:c.2228_2238del	NM_032160.2:c.2229_2238del	NM_032160.2:c.2230_2238del	NM_032160.2:c.2231_2238del	NM_032160.2:c.2232_2238del	NM_032160.2:c.2233_2238del	NM_032160.2:c.2234_2238del	NM_032160.2:c.2235_2238del	NM_032160.2:c.2236_2238del	NM_032160.2:c.2237_2238del	NM_032160.2:c.*2238del	NM_032160.2:c.*2238dup	NM_032160.2:c.2237_2238dup	NM_032160.2:c.2236_2238dup	NM_032160.2:c.2235_2238dup	NM_032160.2:c.2231_2238dup	NM_032160.2:c.2230_2238dup	NM_032160.2:c.2229_2238dup	NM_032160.2:c.2224_2238dup

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#.

52 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95715454	Feb 13, 2009 (130)
2	HUMANGENOME_JCVI	ss96367578	Feb 16, 2009 (130)
3	PJP	ss294946071	May 09, 2011 (137)
4	PJP	ss294946072	May 09, 2011 (137)
5	SSMP	ss664413742	Apr 01, 2015 (144)
6	BILGI_BIOE	ss666717635	Apr 25, 2013 (138)
7	1000GENOMES	ss1377656984	Aug 21, 2014 (142)
8	EVA_UK10K_ALSPAC	ss1709045608	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1709045610	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1709047399	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1709047402	Apr 01, 2015 (144)
12	SWEGEN	ss3016759353	Nov 08, 2017 (151)
13	URBANLAB	ss3650822024	Oct 12, 2018 (152)
14	KHV_HUMAN_GENOMES	ss3820825775	Jul 13, 2019 (153)
15	EVA	ss3835244697	Apr 27, 2020 (154)
16	VINODS	ss4033545776	Apr 27, 2021 (155)
17	GNOMAD	ss4324489041	Apr 27, 2021 (155)
18	GNOMAD	ss4324489042	Apr 27, 2021 (155)
19	GNOMAD	ss4324489043	Apr 27, 2021 (155)
20	GNOMAD	ss4324489044	Apr 27, 2021 (155)
21	GNOMAD	ss4324489045	Apr 27, 2021 (155)
22	GNOMAD	ss4324489046	Apr 27, 2021 (155)
23	GNOMAD	ss4324489047	Apr 27, 2021 (155)
24	GNOMAD	ss4324489048	Apr 27, 2021 (155)
25	GNOMAD	ss4324489050	Apr 27, 2021 (155)
26	GNOMAD	ss4324489051	Apr 27, 2021 (155)
27	GNOMAD	ss4324489052	Apr 27, 2021 (155)
28	GNOMAD	ss4324489053	Apr 27, 2021 (155)
29	GNOMAD	ss4324489054	Apr 27, 2021 (155)
30	GNOMAD	ss4324489055	Apr 27, 2021 (155)
31	GNOMAD	ss4324489056	Apr 27, 2021 (155)
32	GNOMAD	ss4324489057	Apr 27, 2021 (155)
33	TOPMED	ss5061730744	Apr 27, 2021 (155)
34	TOPMED	ss5061730745	Apr 27, 2021 (155)
35	TOMMO_GENOMICS	ss5225810653	Apr 27, 2021 (155)
36	TOMMO_GENOMICS	ss5225810654	Apr 27, 2021 (155)
37	TOMMO_GENOMICS	ss5225810655	Apr 27, 2021 (155)
38	TOMMO_GENOMICS	ss5225810656	Apr 27, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5305792801	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5305792802	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5498515344	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5498515345	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5498515346	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5498515347	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5498515348	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5783785289	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5783785290	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5783785292	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5783785293	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5783785294	Oct 16, 2022 (156)
51	TMC_SNPDB2	ss5847102307	Oct 16, 2022 (156)
52	EVA	ss5852117599	Oct 16, 2022 (156)
53	1000Genomes	NC_000018.9 - 65175969	Oct 12, 2018 (152)
54	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 41541681 (NC_000018.9:65175968::TT 807/3854) Row 41541682 (NC_000018.9:65175968::T 1601/3854)	-	Oct 12, 2018 (152)
55	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 41541681 (NC_000018.9:65175968::TT 807/3854) Row 41541682 (NC_000018.9:65175968::T 1601/3854)	-	Oct 12, 2018 (152)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 528661592 (NC_000018.10:67508731::T 53415/116194) Row 528661593 (NC_000018.10:67508731::TT 16856/116344) Row 528661594 (NC_000018.10:67508731::TTT 577/116408)...	-	Apr 27, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 83779960 (NC_000018.9:65175968::T 8013/16504) Row 83779961 (NC_000018.9:65175968::TT 2592/16504) Row 83779962 (NC_000018.9:65175968::TTT 7/16504)...	-	Apr 27, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 83779960 (NC_000018.9:65175968::T 8013/16504) Row 83779961 (NC_000018.9:65175968::TT 2592/16504) Row 83779962 (NC_000018.9:65175968::TTT 7/16504)...	-	Apr 27, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 83779960 (NC_000018.9:65175968::T 8013/16504) Row 83779961 (NC_000018.9:65175968::TT 2592/16504) Row 83779962 (NC_000018.9:65175968::TTT 7/16504)...	-	Apr 27, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 83779960 (NC_000018.9:65175968::T 8013/16504) Row 83779961 (NC_000018.9:65175968::TT 2592/16504) Row 83779962 (NC_000018.9:65175968::TTT 7/16504)...	-	Apr 27, 2021 (155)
76	14KJPN Submission ignored due to conflicting rows: Row 117622393 (NC_000018.10:67508731::T 12137/26522) Row 117622394 (NC_000018.10:67508731:T: 3/26522) Row 117622396 (NC_000018.10:67508731::TT 3708/26522)...	-	Oct 16, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 117622393 (NC_000018.10:67508731::T 12137/26522) Row 117622394 (NC_000018.10:67508731:T: 3/26522) Row 117622396 (NC_000018.10:67508731::TT 3708/26522)...	-	Oct 16, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 117622393 (NC_000018.10:67508731::T 12137/26522) Row 117622394 (NC_000018.10:67508731:T: 3/26522) Row 117622396 (NC_000018.10:67508731::TT 3708/26522)...	-	Oct 16, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 117622393 (NC_000018.10:67508731::T 12137/26522) Row 117622394 (NC_000018.10:67508731:T: 3/26522) Row 117622396 (NC_000018.10:67508731::TT 3708/26522)...	-	Oct 16, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 117622393 (NC_000018.10:67508731::T 12137/26522) Row 117622394 (NC_000018.10:67508731:T: 3/26522) Row 117622396 (NC_000018.10:67508731::TT 3708/26522)...	-	Oct 16, 2022 (156)
81	TopMed Submission ignored due to conflicting rows: Row 277276407 (NC_000018.10:67508731:TTTTTT: 14/264690) Row 277276408 (NC_000018.10:67508731:TTTTTTTTT: 1/264690)	-	Apr 27, 2021 (155)
82	TopMed Submission ignored due to conflicting rows: Row 277276407 (NC_000018.10:67508731:TTTTTT: 14/264690) Row 277276408 (NC_000018.10:67508731:TTTTTTTTT: 1/264690)	-	Apr 27, 2021 (155)
83	UK 10K study - Twins Submission ignored due to conflicting rows: Row 41541681 (NC_000018.9:65175968::TT 735/3708) Row 41541682 (NC_000018.9:65175968::T 1599/3708)	-	Oct 12, 2018 (152)
84	UK 10K study - Twins Submission ignored due to conflicting rows: Row 41541681 (NC_000018.9:65175968::TT 735/3708) Row 41541682 (NC_000018.9:65175968::T 1599/3708)	-	Oct 12, 2018 (152)
85	ALFA	NC_000018.10 - 67508732	Apr 27, 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)
rs145058215	May 04, 2012 (137)
rs72356655	Jul 30, 2012 (137)
rs72464470	Jul 30, 2012 (137)
rs149938168	May 04, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTT	(self)
ss5225810656	NC_000018.9:65175968:TTTTTTTTT:	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTT	(self)
ss4324489057, ss5061730745, ss5783785294	NC_000018.10:67508731:TTTTTTTTT:	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTT	(self)
ss4324489056	NC_000018.10:67508731:TTTTTTTT:	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss3016759353	NC_000018.9:65175968:TTTTTTT:	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4324489055	NC_000018.10:67508731:TTTTTTT:	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4324489054, ss5061730744	NC_000018.10:67508731:TTTTTT:	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4324489053	NC_000018.10:67508731:TTTT:	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4324489052, ss5498515348	NC_000018.10:67508731:TTT:	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4324489051	NC_000018.10:67508731:TT:	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4324489050, ss5498515346, ss5783785290	NC_000018.10:67508731:T:	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss294946071	NC_000018.8:63326949::T	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss294946072	NC_000018.8:63326964::T	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
74947887, ss666717635, ss1377656984, ss1709045610, ss1709047402, ss3835244697, ss5225810653	NC_000018.9:65175968::T	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3650822024, ss3820825775, ss4324489041, ss5305792801, ss5498515344, ss5783785289, ss5852117599	NC_000018.10:67508731::T	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4033545776	NW_003315960.1:154458::T	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss664413742, ss1709045608, ss1709047399, ss5225810654	NC_000018.9:65175968::TT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4324489042, ss5305792802, ss5498515345, ss5783785292	NC_000018.10:67508731::TT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss96367578	NT_025028.14:12966832::TT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss95715454	NT_025028.14:12966848::TT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5225810655	NC_000018.9:65175968::TTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4324489043, ss5498515347, ss5783785293	NC_000018.10:67508731::TTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4324489044, ss5847102307	NC_000018.10:67508731::TTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4324489045	NC_000018.10:67508731::TTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4324489046	NC_000018.10:67508731::TTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4324489047	NC_000018.10:67508731::TTTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4324489048	NC_000018.10:67508731::TTTTTTTTTTT… NC_000018.10:67508731::TTTTTTTTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1310167789	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2388170710	NC_000018.9:65175968:TTT:	NC_000018.10:67508731:TTTTTTTTTTTT… NC_000018.10:67508731:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT

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

No publications for rs71171183

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

rs71171183