Name: rs36075624
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.

rs36075624

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:86602941-86602961 (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(A)₉ / del(A)₈ / del(A)₇ / del(…
del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₈ / dup(A)₁₄ / dup(A)₁₅ / dup(A)₁₆ / dup(A)₁₇ / dup(A)₁₈ / dup(A)₁₉ / dup(A)₂₁ / ins(A)₂₂ / ins(A)₂₃ / ins(A)₃₀
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₉=0.0000 (0/4092, ALFA)
del(A)₈=0.0000 (0/4092, ALFA)
del(A)₇=0.0000 (0/4092, ALFA) (+ 9 more)
del(A)₆=0.0000 (0/4092, ALFA)
del(A)₅=0.0000 (0/4092, ALFA)
del(A)₄=0.0000 (0/4092, ALFA)
delAA=0.0000 (0/4092, ALFA)
delA=0.0000 (0/4092, ALFA)
dupA=0.0000 (0/4092, ALFA)
dupAA=0.0000 (0/4092, ALFA)
dupAAA=0.0000 (0/4092, ALFA)
dup(A)₆=0.0000 (0/4092, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CHMP3-AS1 : Intron Variant
RNF103-CHMP3 : Intron Variant
RNF103 : 500B Downstream 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	4092	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	2064	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African	Sub	1692	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	72	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1620	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	2	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	60	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	108	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	20	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	146	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A

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	4092	(A)₂₁=1.0000	del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	European	Sub	2064	(A)₂₁=1.0000	del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	African	Sub	1692	(A)₂₁=1.0000	del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	Other	Sub	146	(A)₂₁=1.000	del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	108	(A)₂₁=1.000	del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	60	(A)₂₁=1.00	del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	20	(A)₂₁=1.00	del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	Asian	Sub	2	(A)₂₁=1.0	del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₆=0.0

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 2	NC_000002.12:g.86602953_86602961del
GRCh38.p14 chr 2	NC_000002.12:g.86602954_86602961del
GRCh38.p14 chr 2	NC_000002.12:g.86602955_86602961del
GRCh38.p14 chr 2	NC_000002.12:g.86602956_86602961del
GRCh38.p14 chr 2	NC_000002.12:g.86602957_86602961del
GRCh38.p14 chr 2	NC_000002.12:g.86602958_86602961del
GRCh38.p14 chr 2	NC_000002.12:g.86602960_86602961del
GRCh38.p14 chr 2	NC_000002.12:g.86602961del
GRCh38.p14 chr 2	NC_000002.12:g.86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602960_86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602959_86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602958_86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602957_86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602956_86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602955_86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602954_86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602948_86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602947_86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602946_86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602945_86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602944_86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602943_86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602941_86602961dup
GRCh38.p14 chr 2	NC_000002.12:g.86602961_86602962insAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 2	NC_000002.12:g.86602961_86602962insAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 2	NC_000002.12:g.86602961_86602962insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 2	NC_000002.11:g.86830076_86830084del
GRCh37.p13 chr 2	NC_000002.11:g.86830077_86830084del
GRCh37.p13 chr 2	NC_000002.11:g.86830078_86830084del
GRCh37.p13 chr 2	NC_000002.11:g.86830079_86830084del
GRCh37.p13 chr 2	NC_000002.11:g.86830080_86830084del
GRCh37.p13 chr 2	NC_000002.11:g.86830081_86830084del
GRCh37.p13 chr 2	NC_000002.11:g.86830083_86830084del
GRCh37.p13 chr 2	NC_000002.11:g.86830084del
GRCh37.p13 chr 2	NC_000002.11:g.86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830083_86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830082_86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830081_86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830080_86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830079_86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830078_86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830077_86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830071_86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830070_86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830069_86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830068_86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830067_86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830066_86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830064_86830084dup
GRCh37.p13 chr 2	NC_000002.11:g.86830084_86830085insAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 2	NC_000002.11:g.86830084_86830085insAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 2	NC_000002.11:g.86830084_86830085insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: RNF103-CHMP3, RNF103-CHMP3 readthrough (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RNF103-CHMP3 transcript	NM_001198954.1:c.132+1738… NM_001198954.1:c.132+17381_132+17389del	N/A	Intron Variant

Gene: RNF103, ring finger protein 103 (minus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
RNF103 transcript variant 2	NM_001198951.1:c.	N/A	Downstream Transcript Variant
RNF103 transcript variant 1	NM_005667.4:c.	N/A	Downstream Transcript Variant
RNF103 transcript variant 3	NM_001198952.2:c.	N/A	N/A

Gene: CHMP3-AS1, uncharacterized CHMP3-AS1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CHMP3-AS1 transcript variant X1	XR_940320.4: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	(A)₂₁=	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₈	dup(A)₁₄	dup(A)₁₅	dup(A)₁₆	dup(A)₁₇	dup(A)₁₈	dup(A)₁₉	dup(A)₂₁	ins(A)₂₂	ins(A)₂₃	ins(A)₃₀
GRCh38.p14 chr 2	NC_000002.12:g.86602941_86602961=	NC_000002.12:g.86602953_86602961del	NC_000002.12:g.86602954_86602961del	NC_000002.12:g.86602955_86602961del	NC_000002.12:g.86602956_86602961del	NC_000002.12:g.86602957_86602961del	NC_000002.12:g.86602958_86602961del	NC_000002.12:g.86602960_86602961del	NC_000002.12:g.86602961del	NC_000002.12:g.86602961dup	NC_000002.12:g.86602960_86602961dup	NC_000002.12:g.86602959_86602961dup	NC_000002.12:g.86602958_86602961dup	NC_000002.12:g.86602957_86602961dup	NC_000002.12:g.86602956_86602961dup	NC_000002.12:g.86602955_86602961dup	NC_000002.12:g.86602954_86602961dup	NC_000002.12:g.86602948_86602961dup	NC_000002.12:g.86602947_86602961dup	NC_000002.12:g.86602946_86602961dup	NC_000002.12:g.86602945_86602961dup	NC_000002.12:g.86602944_86602961dup	NC_000002.12:g.86602943_86602961dup	NC_000002.12:g.86602941_86602961dup	NC_000002.12:g.86602961_86602962insAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:g.86602961_86602962insAAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:g.86602961_86602962insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 2	NC_000002.11:g.86830064_86830084=	NC_000002.11:g.86830076_86830084del	NC_000002.11:g.86830077_86830084del	NC_000002.11:g.86830078_86830084del	NC_000002.11:g.86830079_86830084del	NC_000002.11:g.86830080_86830084del	NC_000002.11:g.86830081_86830084del	NC_000002.11:g.86830083_86830084del	NC_000002.11:g.86830084del	NC_000002.11:g.86830084dup	NC_000002.11:g.86830083_86830084dup	NC_000002.11:g.86830082_86830084dup	NC_000002.11:g.86830081_86830084dup	NC_000002.11:g.86830080_86830084dup	NC_000002.11:g.86830079_86830084dup	NC_000002.11:g.86830078_86830084dup	NC_000002.11:g.86830077_86830084dup	NC_000002.11:g.86830071_86830084dup	NC_000002.11:g.86830070_86830084dup	NC_000002.11:g.86830069_86830084dup	NC_000002.11:g.86830068_86830084dup	NC_000002.11:g.86830067_86830084dup	NC_000002.11:g.86830066_86830084dup	NC_000002.11:g.86830064_86830084dup	NC_000002.11:g.86830084_86830085insAAAAAAAAAAAAAAAAAAAAAA	NC_000002.11:g.86830084_86830085insAAAAAAAAAAAAAAAAAAAAAAA	NC_000002.11:g.86830084_86830085insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
RNF103-CHMP3 transcript	NM_001198954.1:c.132+17389=	NM_001198954.1:c.132+17381_132+17389del	NM_001198954.1:c.132+17382_132+17389del	NM_001198954.1:c.132+17383_132+17389del	NM_001198954.1:c.132+17384_132+17389del	NM_001198954.1:c.132+17385_132+17389del	NM_001198954.1:c.132+17386_132+17389del	NM_001198954.1:c.132+17388_132+17389del	NM_001198954.1:c.132+17389del	NM_001198954.1:c.132+17389dup	NM_001198954.1:c.132+17388_132+17389dup	NM_001198954.1:c.132+17387_132+17389dup	NM_001198954.1:c.132+17386_132+17389dup	NM_001198954.1:c.132+17385_132+17389dup	NM_001198954.1:c.132+17384_132+17389dup	NM_001198954.1:c.132+17383_132+17389dup	NM_001198954.1:c.132+17382_132+17389dup	NM_001198954.1:c.132+17376_132+17389dup	NM_001198954.1:c.132+17375_132+17389dup	NM_001198954.1:c.132+17374_132+17389dup	NM_001198954.1:c.132+17373_132+17389dup	NM_001198954.1:c.132+17372_132+17389dup	NM_001198954.1:c.132+17371_132+17389dup	NM_001198954.1:c.132+17369_132+17389dup	NM_001198954.1:c.132+17389_132+17390insTTTTTTTTTTTTTTTTTTTTTT	NM_001198954.1:c.132+17389_132+17390insTTTTTTTTTTTTTTTTTTTTTTT	NM_001198954.1:c.132+17389_132+17390insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

56 SubSNP, 34 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41655416	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss95278768	Dec 05, 2013 (138)
3	PJP	ss294993142	May 09, 2011 (138)
4	SSMP	ss663333258	Apr 01, 2015 (144)
5	SWEGEN	ss2989897482	Nov 08, 2017 (151)
6	SWEGEN	ss2989897484	Nov 08, 2017 (151)
7	SWEGEN	ss2989897485	Nov 08, 2017 (151)
8	SWEGEN	ss2989897486	Nov 08, 2017 (151)
9	URBANLAB	ss3647081754	Oct 11, 2018 (152)
10	EVA_DECODE	ss3704371038	Jul 13, 2019 (153)
11	EVA_DECODE	ss3704371039	Jul 13, 2019 (153)
12	EVA_DECODE	ss3704371040	Jul 13, 2019 (153)
13	EVA_DECODE	ss3704371041	Jul 13, 2019 (153)
14	EVA_DECODE	ss3704371042	Jul 13, 2019 (153)
15	EVA	ss3827101199	Apr 25, 2020 (154)
16	GNOMAD	ss4045628259	Apr 26, 2021 (155)
17	GNOMAD	ss4045628260	Apr 26, 2021 (155)
18	GNOMAD	ss4045628261	Apr 26, 2021 (155)
19	GNOMAD	ss4045628262	Apr 26, 2021 (155)
20	GNOMAD	ss4045628263	Apr 26, 2021 (155)
21	GNOMAD	ss4045628264	Apr 26, 2021 (155)
22	GNOMAD	ss4045628265	Apr 26, 2021 (155)
23	GNOMAD	ss4045628266	Apr 26, 2021 (155)
24	GNOMAD	ss4045628267	Apr 26, 2021 (155)
25	GNOMAD	ss4045628268	Apr 26, 2021 (155)
26	GNOMAD	ss4045628269	Apr 26, 2021 (155)
27	GNOMAD	ss4045628270	Apr 26, 2021 (155)
28	GNOMAD	ss4045628271	Apr 26, 2021 (155)
29	GNOMAD	ss4045628272	Apr 26, 2021 (155)
30	GNOMAD	ss4045628273	Apr 26, 2021 (155)
31	GNOMAD	ss4045628274	Apr 26, 2021 (155)
32	GNOMAD	ss4045628275	Apr 26, 2021 (155)
33	GNOMAD	ss4045628277	Apr 26, 2021 (155)
34	GNOMAD	ss4045628278	Apr 26, 2021 (155)
35	GNOMAD	ss4045628279	Apr 26, 2021 (155)
36	GNOMAD	ss4045628280	Apr 26, 2021 (155)
37	GNOMAD	ss4045628281	Apr 26, 2021 (155)
38	GNOMAD	ss4045628282	Apr 26, 2021 (155)
39	GNOMAD	ss4045628283	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5152474055	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5152474056	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5152474057	Apr 26, 2021 (155)
43	1000G_HIGH_COVERAGE	ss5248918474	Oct 12, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5248918475	Oct 12, 2022 (156)
45	HUGCELL_USP	ss5449037692	Oct 12, 2022 (156)
46	HUGCELL_USP	ss5449037693	Oct 12, 2022 (156)
47	HUGCELL_USP	ss5449037694	Oct 12, 2022 (156)
48	HUGCELL_USP	ss5449037695	Oct 12, 2022 (156)
49	HUGCELL_USP	ss5449037696	Oct 12, 2022 (156)
50	TOMMO_GENOMICS	ss5681414254	Oct 12, 2022 (156)
51	TOMMO_GENOMICS	ss5681414256	Oct 12, 2022 (156)
52	TOMMO_GENOMICS	ss5681414257	Oct 12, 2022 (156)
53	TOMMO_GENOMICS	ss5681414258	Oct 12, 2022 (156)
54	TOMMO_GENOMICS	ss5681414259	Oct 12, 2022 (156)
55	EVA	ss5820424844	Oct 12, 2022 (156)
56	EVA	ss5820424845	Oct 12, 2022 (156)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65349875 (NC_000002.12:86602940::A 30869/54784) Row 65349876 (NC_000002.12:86602940::AA 314/54430) Row 65349877 (NC_000002.12:86602940::AAA 192/54420)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 10443362 (NC_000002.11:86830063::A 10457/15360) Row 10443363 (NC_000002.11:86830063::AA 33/15360) Row 10443364 (NC_000002.11:86830063::AAA 23/15360)	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 10443362 (NC_000002.11:86830063::A 10457/15360) Row 10443363 (NC_000002.11:86830063::AA 33/15360) Row 10443364 (NC_000002.11:86830063::AAA 23/15360)	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 10443362 (NC_000002.11:86830063::A 10457/15360) Row 10443363 (NC_000002.11:86830063::AA 33/15360) Row 10443364 (NC_000002.11:86830063::AAA 23/15360)	-	Apr 26, 2021 (155)
85	14KJPN Submission ignored due to conflicting rows: Row 15251358 (NC_000002.12:86602940::A 19803/27452) Row 15251360 (NC_000002.12:86602940::AA 43/27452) Row 15251361 (NC_000002.12:86602940:A: 9/27452)...	-	Oct 12, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 15251358 (NC_000002.12:86602940::A 19803/27452) Row 15251360 (NC_000002.12:86602940::AA 43/27452) Row 15251361 (NC_000002.12:86602940:A: 9/27452)...	-	Oct 12, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 15251358 (NC_000002.12:86602940::A 19803/27452) Row 15251360 (NC_000002.12:86602940::AA 43/27452) Row 15251361 (NC_000002.12:86602940:A: 9/27452)...	-	Oct 12, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 15251358 (NC_000002.12:86602940::A 19803/27452) Row 15251360 (NC_000002.12:86602940::AA 43/27452) Row 15251361 (NC_000002.12:86602940:A: 9/27452)...	-	Oct 12, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 15251358 (NC_000002.12:86602940::A 19803/27452) Row 15251360 (NC_000002.12:86602940::AA 43/27452) Row 15251361 (NC_000002.12:86602940:A: 9/27452)...	-	Oct 12, 2022 (156)
90	ALFA	NC_000002.12 - 86602941	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)
rs70956194	May 15, 2013 (138)
rs71792842	May 11, 2012 (137)
rs71869419	May 11, 2012 (137)
rs72404861	May 11, 2012 (137)
rs150518473	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4045628283	NC_000002.12:86602940:AAAAAAAAA:	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
536614940	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4045628282	NC_000002.12:86602940:AAAAAAAA:	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
536614940	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4045628281	NC_000002.12:86602940:AAAAAAA:	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
536614940	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4045628280	NC_000002.12:86602940:AAAAAA:	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
536614940	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4045628279	NC_000002.12:86602940:AAAAA:	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
536614940	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4045628278	NC_000002.12:86602940:AAAA:	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
536614940	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3704371042, ss4045628277	NC_000002.12:86602940:AA:	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
536614940	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5248918474, ss5449037694, ss5681414257	NC_000002.12:86602940:A:	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
536614940	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3704371041	NC_000002.12:86602941:A:	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss294993142	NC_000002.10:86683595::A	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss663333258, ss2989897482, ss3827101199, ss5152474055	NC_000002.11:86830063::A	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3647081754, ss4045628259, ss5449037692, ss5681414254	NC_000002.12:86602940::A	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
536614940	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3704371040	NC_000002.12:86602942::A	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss41655416	NT_022184.15:65651950::A	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss95278768	NT_022184.15:65651971::A	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5152474056, ss5820424844	NC_000002.11:86830063::AA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628260, ss5248918475, ss5449037693, ss5681414256	NC_000002.12:86602940::AA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
536614940	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3704371039	NC_000002.12:86602942::AA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss2989897484, ss5152474057, ss5820424845	NC_000002.11:86830063::AAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628261, ss5681414258	NC_000002.12:86602940::AAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
536614940	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628262	NC_000002.12:86602940::AAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628263	NC_000002.12:86602940::AAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3704371038	NC_000002.12:86602942::AAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss2989897485	NC_000002.11:86830063::AAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628264, ss5449037695	NC_000002.12:86602940::AAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
536614940	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628265, ss5449037696, ss5681414259	NC_000002.12:86602940::AAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628266	NC_000002.12:86602940::AAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628267	NC_000002.12:86602940::AAAAAAAAAAA… NC_000002.12:86602940::AAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628268	NC_000002.12:86602940::AAAAAAAAAAA… NC_000002.12:86602940::AAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628269	NC_000002.12:86602940::AAAAAAAAAAA… NC_000002.12:86602940::AAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628270	NC_000002.12:86602940::AAAAAAAAAAA… NC_000002.12:86602940::AAAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628271	NC_000002.12:86602940::AAAAAAAAAAA… NC_000002.12:86602940::AAAAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628272	NC_000002.12:86602940::AAAAAAAAAAA… NC_000002.12:86602940::AAAAAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628273	NC_000002.12:86602940::AAAAAAAAAAA… NC_000002.12:86602940::AAAAAAAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628274	NC_000002.12:86602940::AAAAAAAAAAA… NC_000002.12:86602940::AAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss2989897486	NC_000002.11:86830063::AAAAAAAAAAA… NC_000002.11:86830063::AAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4045628275	NC_000002.12:86602940::AAAAAAAAAAA… NC_000002.12:86602940::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:86602940:AAAAAAAAAAAA… NC_000002.12:86602940:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs36075624

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

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs36075624