Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

dbSNP Short Genetic Variations

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.

rs754665666

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr4:188454531-188454557 (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(CA)5 / del(CA)4 / del(CA)3 / d…

del(CA)5 / del(CA)4 / del(CA)3 / delCACA / delCA / dupCA / dupCACA / dup(CA)3 / dup(CA)4 / dup(CA)5 / dup(CA)6 / dup(CA)7 / dup(CA)8 / dup(CA)9 / dup(CA)10 / dup(CA)11 / dup(CA)12 / dup(CA)13 / ins(CA)14

Variation Type
Indel Insertion and Deletion
Frequency
delCA=0.01648 (216/13110, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
LINC01060 : 2KB Upstream Variant
LOC105377609 : 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 13110 ACACACACACACACACACACACACACA=0.98169 ACACACACACACACACACA=0.00000, ACACACACACACACACACACA=0.00015, ACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACA=0.01648, ACACACACACACACACACACACACACACA=0.00122, ACACACACACACACACACACACACACACACACACACA=0.00031, ACACACACACACACACACACACACACACACACACACACACACACA=0.00015, ACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACACACACACACA=0.00000 0.971795 0.000321 0.027885 0
European Sub 10339 ACACACACACACACACACACACACACA=0.97679 ACACACACACACACACACA=0.00000, ACACACACACACACACACACA=0.00019, ACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACA=0.02089, ACACACACACACACACACACACACACACA=0.00155, ACACACACACACACACACACACACACACACACACACA=0.00039, ACACACACACACACACACACACACACACACACACACACACACACA=0.00019, ACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACACACACACACA=0.00000 0.963749 0.000412 0.035839 0
African Sub 1624 ACACACACACACACACACACACACACA=1.0000 ACACACACACACACACACA=0.0000, ACACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACACACACACA=0.0000 1.0 0.0 0.0 N/A
African Others Sub 56 ACACACACACACACACACACACACACA=1.00 ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACACACA=0.00 1.0 0.0 0.0 N/A
African American Sub 1568 ACACACACACACACACACACACACACA=1.0000 ACACACACACACACACACA=0.0000, ACACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACACACACACA=0.0000 1.0 0.0 0.0 N/A
Asian Sub 104 ACACACACACACACACACACACACACA=1.000 ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACACACACA=0.000 1.0 0.0 0.0 N/A
East Asian Sub 82 ACACACACACACACACACACACACACA=1.00 ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACACACA=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 22 ACACACACACACACACACACACACACA=1.00 ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACACACA=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 122 ACACACACACACACACACACACACACA=1.000 ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACACACACA=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 496 ACACACACACACACACACACACACACA=1.000 ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACACACACA=0.000 1.0 0.0 0.0 N/A
South Asian Sub 76 ACACACACACACACACACACACACACA=1.00 ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACACACA=0.00 1.0 0.0 0.0 N/A
Other Sub 349 ACACACACACACACACACACACACACA=1.000 ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACACACACA=0.000 1.0 0.0 0.0 N/A


Help

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").

Download
Study Population Group Sample Size Ref Allele Alt Allele
Allele Frequency Aggregator Total Global 13110 (AC)13A=0.98169 del(CA)4=0.00000, del(CA)3=0.00015, delCACA=0.00000, delCA=0.01648, dupCA=0.00122, dupCACA=0.00000, dup(CA)3=0.00000, dup(CA)4=0.00000, dup(CA)5=0.00031, dup(CA)6=0.00000, dup(CA)7=0.00000, dup(CA)8=0.00000, dup(CA)9=0.00015, dup(CA)10=0.00000
Allele Frequency Aggregator European Sub 10339 (AC)13A=0.97679 del(CA)4=0.00000, del(CA)3=0.00019, delCACA=0.00000, delCA=0.02089, dupCA=0.00155, dupCACA=0.00000, dup(CA)3=0.00000, dup(CA)4=0.00000, dup(CA)5=0.00039, dup(CA)6=0.00000, dup(CA)7=0.00000, dup(CA)8=0.00000, dup(CA)9=0.00019, dup(CA)10=0.00000
Allele Frequency Aggregator African Sub 1624 (AC)13A=1.0000 del(CA)4=0.0000, del(CA)3=0.0000, delCACA=0.0000, delCA=0.0000, dupCA=0.0000, dupCACA=0.0000, dup(CA)3=0.0000, dup(CA)4=0.0000, dup(CA)5=0.0000, dup(CA)6=0.0000, dup(CA)7=0.0000, dup(CA)8=0.0000, dup(CA)9=0.0000, dup(CA)10=0.0000
Allele Frequency Aggregator Latin American 2 Sub 496 (AC)13A=1.000 del(CA)4=0.000, del(CA)3=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)3=0.000, dup(CA)4=0.000, dup(CA)5=0.000, dup(CA)6=0.000, dup(CA)7=0.000, dup(CA)8=0.000, dup(CA)9=0.000, dup(CA)10=0.000
Allele Frequency Aggregator Other Sub 349 (AC)13A=1.000 del(CA)4=0.000, del(CA)3=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)3=0.000, dup(CA)4=0.000, dup(CA)5=0.000, dup(CA)6=0.000, dup(CA)7=0.000, dup(CA)8=0.000, dup(CA)9=0.000, dup(CA)10=0.000
Allele Frequency Aggregator Latin American 1 Sub 122 (AC)13A=1.000 del(CA)4=0.000, del(CA)3=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)3=0.000, dup(CA)4=0.000, dup(CA)5=0.000, dup(CA)6=0.000, dup(CA)7=0.000, dup(CA)8=0.000, dup(CA)9=0.000, dup(CA)10=0.000
Allele Frequency Aggregator Asian Sub 104 (AC)13A=1.000 del(CA)4=0.000, del(CA)3=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)3=0.000, dup(CA)4=0.000, dup(CA)5=0.000, dup(CA)6=0.000, dup(CA)7=0.000, dup(CA)8=0.000, dup(CA)9=0.000, dup(CA)10=0.000
Allele Frequency Aggregator South Asian Sub 76 (AC)13A=1.00 del(CA)4=0.00, del(CA)3=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)3=0.00, dup(CA)4=0.00, dup(CA)5=0.00, dup(CA)6=0.00, dup(CA)7=0.00, dup(CA)8=0.00, dup(CA)9=0.00, dup(CA)10=0.00
Help

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 4 NC_000004.12:g.188454532CA[8]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[9]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[10]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[11]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[12]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[14]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[15]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[16]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[17]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[18]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[19]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[20]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[21]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[22]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[23]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[24]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[25]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[26]
GRCh38.p14 chr 4 NC_000004.12:g.188454532CA[27]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[8]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[9]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[10]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[11]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[12]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[14]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[15]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[16]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[17]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[18]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[19]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[20]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[21]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[22]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[23]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[24]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[25]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[26]
GRCh37.p13 chr 4 NC_000004.11:g.189375686CA[27]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[8]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[9]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[10]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[11]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[12]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[14]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[15]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[16]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[17]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[18]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[19]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[20]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[21]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[22]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[23]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[24]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[25]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[26]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113110CA[27]
Gene: LINC01060, long intergenic non-protein coding RNA 1060 (plus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
LINC01060 transcript NR_033869.1:n. N/A Upstream Transcript Variant
Gene: LOC105377609, uncharacterized LOC105377609 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
LOC105377609 transcript variant X2 XR_001741960.2:n. N/A Intron Variant
LOC105377609 transcript variant X1 XR_939621.3:n. N/A Intron Variant
Help

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
Help

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 (AC)13A= del(CA)5 del(CA)4 del(CA)3 delCACA delCA dupCA dupCACA dup(CA)3 dup(CA)4 dup(CA)5 dup(CA)6 dup(CA)7 dup(CA)8 dup(CA)9 dup(CA)10 dup(CA)11 dup(CA)12 dup(CA)13 ins(CA)14
GRCh38.p14 chr 4 NC_000004.12:g.188454531_188454557= NC_000004.12:g.188454532CA[8] NC_000004.12:g.188454532CA[9] NC_000004.12:g.188454532CA[10] NC_000004.12:g.188454532CA[11] NC_000004.12:g.188454532CA[12] NC_000004.12:g.188454532CA[14] NC_000004.12:g.188454532CA[15] NC_000004.12:g.188454532CA[16] NC_000004.12:g.188454532CA[17] NC_000004.12:g.188454532CA[18] NC_000004.12:g.188454532CA[19] NC_000004.12:g.188454532CA[20] NC_000004.12:g.188454532CA[21] NC_000004.12:g.188454532CA[22] NC_000004.12:g.188454532CA[23] NC_000004.12:g.188454532CA[24] NC_000004.12:g.188454532CA[25] NC_000004.12:g.188454532CA[26] NC_000004.12:g.188454532CA[27]
GRCh37.p13 chr 4 NC_000004.11:g.189375685_189375711= NC_000004.11:g.189375686CA[8] NC_000004.11:g.189375686CA[9] NC_000004.11:g.189375686CA[10] NC_000004.11:g.189375686CA[11] NC_000004.11:g.189375686CA[12] NC_000004.11:g.189375686CA[14] NC_000004.11:g.189375686CA[15] NC_000004.11:g.189375686CA[16] NC_000004.11:g.189375686CA[17] NC_000004.11:g.189375686CA[18] NC_000004.11:g.189375686CA[19] NC_000004.11:g.189375686CA[20] NC_000004.11:g.189375686CA[21] NC_000004.11:g.189375686CA[22] NC_000004.11:g.189375686CA[23] NC_000004.11:g.189375686CA[24] NC_000004.11:g.189375686CA[25] NC_000004.11:g.189375686CA[26] NC_000004.11:g.189375686CA[27]
GRCh38.p14 chr 4 alt locus HSCHR4_5_CTG12 NT_187545.1:g.113109_113135= NT_187545.1:g.113110CA[8] NT_187545.1:g.113110CA[9] NT_187545.1:g.113110CA[10] NT_187545.1:g.113110CA[11] NT_187545.1:g.113110CA[12] NT_187545.1:g.113110CA[14] NT_187545.1:g.113110CA[15] NT_187545.1:g.113110CA[16] NT_187545.1:g.113110CA[17] NT_187545.1:g.113110CA[18] NT_187545.1:g.113110CA[19] NT_187545.1:g.113110CA[20] NT_187545.1:g.113110CA[21] NT_187545.1:g.113110CA[22] NT_187545.1:g.113110CA[23] NT_187545.1:g.113110CA[24] NT_187545.1:g.113110CA[25] NT_187545.1:g.113110CA[26] NT_187545.1:g.113110CA[27]
Help

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#.

44 SubSNP, 32 Frequency submissions
No Submitter Submission ID Date (Build)
1 SSMP ss663493107 Apr 01, 2015 (144)
2 EVA_DECODE ss3713901777 Jul 13, 2019 (153)
3 EVA_DECODE ss3713901778 Jul 13, 2019 (153)
4 EVA_DECODE ss3713901779 Jul 13, 2019 (153)
5 EVA_DECODE ss3713901780 Jul 13, 2019 (153)
6 EVA_DECODE ss3713901781 Jul 13, 2019 (153)
7 EVA_DECODE ss3713901782 Jul 13, 2019 (153)
8 ACPOP ss3731992143 Jul 13, 2019 (153)
9 ACPOP ss3731992144 Jul 13, 2019 (153)
10 GNOMAD ss4097652766 Apr 26, 2021 (155)
11 GNOMAD ss4097652767 Apr 26, 2021 (155)
12 GNOMAD ss4097652768 Apr 26, 2021 (155)
13 GNOMAD ss4097652769 Apr 26, 2021 (155)
14 GNOMAD ss4097652770 Apr 26, 2021 (155)
15 GNOMAD ss4097652771 Apr 26, 2021 (155)
16 GNOMAD ss4097652772 Apr 26, 2021 (155)
17 GNOMAD ss4097652773 Apr 26, 2021 (155)
18 GNOMAD ss4097652774 Apr 26, 2021 (155)
19 GNOMAD ss4097652775 Apr 26, 2021 (155)
20 GNOMAD ss4097652776 Apr 26, 2021 (155)
21 GNOMAD ss4097652777 Apr 26, 2021 (155)
22 GNOMAD ss4097652778 Apr 26, 2021 (155)
23 GNOMAD ss4097652779 Apr 26, 2021 (155)
24 GNOMAD ss4097652781 Apr 26, 2021 (155)
25 GNOMAD ss4097652782 Apr 26, 2021 (155)
26 GNOMAD ss4097652783 Apr 26, 2021 (155)
27 GNOMAD ss4097652784 Apr 26, 2021 (155)
28 GNOMAD ss4097652785 Apr 26, 2021 (155)
29 TOPMED ss4646421222 Apr 26, 2021 (155)
30 TOPMED ss4646421223 Apr 26, 2021 (155)
31 TOMMO_GENOMICS ss5169905380 Apr 26, 2021 (155)
32 TOMMO_GENOMICS ss5169905381 Apr 26, 2021 (155)
33 TOMMO_GENOMICS ss5169905382 Apr 26, 2021 (155)
34 TOMMO_GENOMICS ss5169905383 Apr 26, 2021 (155)
35 1000G_HIGH_COVERAGE ss5262511830 Oct 13, 2022 (156)
36 HUGCELL_USP ss5460910409 Oct 13, 2022 (156)
37 HUGCELL_USP ss5460910410 Oct 13, 2022 (156)
38 HUGCELL_USP ss5460910411 Oct 13, 2022 (156)
39 HUGCELL_USP ss5460910412 Oct 13, 2022 (156)
40 HUGCELL_USP ss5460910413 Oct 13, 2022 (156)
41 TOMMO_GENOMICS ss5705421879 Oct 13, 2022 (156)
42 TOMMO_GENOMICS ss5705421880 Oct 13, 2022 (156)
43 TOMMO_GENOMICS ss5705421881 Oct 13, 2022 (156)
44 TOMMO_GENOMICS ss5705421882 Oct 13, 2022 (156)
45 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
46 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
47 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
48 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
49 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
50 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
51 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
52 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
53 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
54 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
55 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
56 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
57 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
58 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
59 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
60 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
61 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
62 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
63 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 177129474 (NC_000004.12:188454530::AC 355/117924)
Row 177129475 (NC_000004.12:188454530::ACAC 840/117916)
Row 177129476 (NC_000004.12:188454530::ACACAC 2124/117886)...

- Apr 26, 2021 (155)
64 Northern Sweden

Submission ignored due to conflicting rows:
Row 5277008 (NC_000004.11:189375684:ACACAC: 2/598)
Row 5277009 (NC_000004.11:189375684:AC: 26/598)

- Jul 13, 2019 (153)
65 Northern Sweden

Submission ignored due to conflicting rows:
Row 5277008 (NC_000004.11:189375684:ACACAC: 2/598)
Row 5277009 (NC_000004.11:189375684:AC: 26/598)

- Jul 13, 2019 (153)
66 8.3KJPN

Submission ignored due to conflicting rows:
Row 27874687 (NC_000004.11:189375684:AC: 252/16730)
Row 27874688 (NC_000004.11:189375684::AC 52/16730)
Row 27874689 (NC_000004.11:189375684::ACACACACACAC 19/16730)...

- Apr 26, 2021 (155)
67 8.3KJPN

Submission ignored due to conflicting rows:
Row 27874687 (NC_000004.11:189375684:AC: 252/16730)
Row 27874688 (NC_000004.11:189375684::AC 52/16730)
Row 27874689 (NC_000004.11:189375684::ACACACACACAC 19/16730)...

- Apr 26, 2021 (155)
68 8.3KJPN

Submission ignored due to conflicting rows:
Row 27874687 (NC_000004.11:189375684:AC: 252/16730)
Row 27874688 (NC_000004.11:189375684::AC 52/16730)
Row 27874689 (NC_000004.11:189375684::ACACACACACAC 19/16730)...

- Apr 26, 2021 (155)
69 8.3KJPN

Submission ignored due to conflicting rows:
Row 27874687 (NC_000004.11:189375684:AC: 252/16730)
Row 27874688 (NC_000004.11:189375684::AC 52/16730)
Row 27874689 (NC_000004.11:189375684::ACACACACACAC 19/16730)...

- Apr 26, 2021 (155)
70 14KJPN

Submission ignored due to conflicting rows:
Row 39258983 (NC_000004.12:188454530::ACACACACACAC 55/28232)
Row 39258984 (NC_000004.12:188454530::AC 84/28232)
Row 39258985 (NC_000004.12:188454530:AC: 413/28232)...

- Oct 13, 2022 (156)
71 14KJPN

Submission ignored due to conflicting rows:
Row 39258983 (NC_000004.12:188454530::ACACACACACAC 55/28232)
Row 39258984 (NC_000004.12:188454530::AC 84/28232)
Row 39258985 (NC_000004.12:188454530:AC: 413/28232)...

- Oct 13, 2022 (156)
72 14KJPN

Submission ignored due to conflicting rows:
Row 39258983 (NC_000004.12:188454530::ACACACACACAC 55/28232)
Row 39258984 (NC_000004.12:188454530::AC 84/28232)
Row 39258985 (NC_000004.12:188454530:AC: 413/28232)...

- Oct 13, 2022 (156)
73 14KJPN

Submission ignored due to conflicting rows:
Row 39258983 (NC_000004.12:188454530::ACACACACACAC 55/28232)
Row 39258984 (NC_000004.12:188454530::AC 84/28232)
Row 39258985 (NC_000004.12:188454530:AC: 413/28232)...

- Oct 13, 2022 (156)
74 TopMed

Submission ignored due to conflicting rows:
Row 483798778 (NC_000004.12:188454530:AC: 19774/264690)
Row 483798779 (NC_000004.12:188454530:ACACACAC: 1/264690)

- Apr 26, 2021 (155)
75 TopMed

Submission ignored due to conflicting rows:
Row 483798778 (NC_000004.12:188454530:AC: 19774/264690)
Row 483798779 (NC_000004.12:188454530:ACACACAC: 1/264690)

- Apr 26, 2021 (155)
76 ALFA NC_000004.12 - 188454531 Apr 26, 2021 (155)
Help

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)
rs370425178 May 13, 2013 (138)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss4097652785 NC_000004.12:188454530:ACACACACAC: NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACA

(self)
ss3713901782, ss4097652784, ss4646421223 NC_000004.12:188454530:ACACACAC: NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACA

(self)
11604820093 NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACA

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACA

(self)
ss3731992143 NC_000004.11:189375684:ACACAC: NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACA

(self)
ss4097652783, ss5460910412 NC_000004.12:188454530:ACACAC: NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACA

(self)
11604820093 NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACA

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACA

(self)
ss3713901781 NC_000004.12:188454532:ACACAC: NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACA

(self)
ss5169905383 NC_000004.11:189375684:ACAC: NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACA

(self)
ss4097652782, ss5460910410, ss5705421882 NC_000004.12:188454530:ACAC: NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACA

(self)
11604820093 NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACA

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACA

(self)
ss3713901780 NC_000004.12:188454534:ACAC: NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACA

(self)
ss663493107, ss3731992144, ss5169905380 NC_000004.11:189375684:AC: NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACA

(self)
ss4097652781, ss4646421222, ss5460910409, ss5705421881 NC_000004.12:188454530:AC: NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACA

(self)
11604820093 NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACA

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACA

(self)
ss3713901779 NC_000004.12:188454536:AC: NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACA

(self)
ss5169905381 NC_000004.11:189375684::AC NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA

(self)
ss4097652766, ss5705421880 NC_000004.12:188454530::AC NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA

(self)
11604820093 NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA

(self)
ss3713901778 NC_000004.12:188454538::AC NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA

(self)
ss4097652767 NC_000004.12:188454530::ACAC NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA

(self)
11604820093 NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA

(self)
ss3713901777 NC_000004.12:188454538::ACAC NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA

(self)
ss4097652768, ss5460910413 NC_000004.12:188454530::ACACAC NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA

(self)
11604820093 NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA

(self)
ss4097652769, ss5460910411 NC_000004.12:188454530::ACACACAC NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA

(self)
11604820093 NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA

(self)
ss4097652770, ss5262511830 NC_000004.12:188454530::ACACACACAC NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA

(self)
11604820093 NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA

(self)
ss5169905382 NC_000004.11:189375684::ACACACACAC…

NC_000004.11:189375684::ACACACACACAC

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACA

(self)
ss4097652771, ss5705421879 NC_000004.12:188454530::ACACACACAC…

NC_000004.12:188454530::ACACACACACAC

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACA

(self)
11604820093 NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACA

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACA

(self)
ss4097652772 NC_000004.12:188454530::ACACACACAC…

NC_000004.12:188454530::ACACACACACACAC

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACA

(self)
11604820093 NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACA

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACA

(self)
ss4097652773 NC_000004.12:188454530::ACACACACAC…

NC_000004.12:188454530::ACACACACACACACAC

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACA

(self)
11604820093 NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACA

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACA

(self)
ss4097652774 NC_000004.12:188454530::ACACACACAC…

NC_000004.12:188454530::ACACACACACACACACAC

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACA

(self)
11604820093 NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACA

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACA

(self)
ss4097652775 NC_000004.12:188454530::ACACACACAC…

NC_000004.12:188454530::ACACACACACACACACACAC

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACA

(self)
11604820093 NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACA

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACA

(self)
ss4097652776 NC_000004.12:188454530::ACACACACAC…

NC_000004.12:188454530::ACACACACACACACACACACAC

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACA

(self)
ss4097652777 NC_000004.12:188454530::ACACACACAC…

NC_000004.12:188454530::ACACACACACACACACACACACAC

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACACA

(self)
ss4097652778 NC_000004.12:188454530::ACACACACAC…

NC_000004.12:188454530::ACACACACACACACACACACACACAC

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACACACA

(self)
ss4097652779 NC_000004.12:188454530::ACACACACAC…

NC_000004.12:188454530::ACACACACACACACACACACACACACAC

NC_000004.12:188454530:ACACACACACA…

NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA

(self)
Help

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

No publications for rs754665666

Help

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.

Software version is: 2.0.1.post820+afb47a3d