Name: rs35550596
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.

rs35550596

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:184911063-184911091 (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)₇ / del(CA)₆ / del(CA)₅ / d…
del(CA)₇ / del(CA)₆ / 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
Variation Type: Indel Insertion and Deletion
Frequency: dupCA=0.03320 (495/14908, ALFA)
dupCA=0.10 (4/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NIBAN1 : 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	14908	ACACACACACACACACACACACACACACA=0.96619	ACACACACACACACA=0.00000, ACACACACACACACACA=0.00000, ACACACACACACACACACA=0.00000, ACACACACACACACACACACA=0.00000, ACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACA=0.00054, ACACACACACACACACACACACACACACACA=0.03320, ACACACACACACACACACACACACACACACACA=0.00007, ACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACACACACA=0.00000	0.938482	0.004835	0.056682	32
European	Sub	12304	ACACACACACACACACACACACACACACA=0.95912	ACACACACACACACA=0.00000, ACACACACACACACACA=0.00000, ACACACACACACACACACA=0.00000, ACACACACACACACACACACA=0.00000, ACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACA=0.00065, ACACACACACACACACACACACACACACACA=0.04015, ACACACACACACACACACACACACACACACACA=0.00008, ACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACACACACACA=0.00000	0.925606	0.00586	0.068533	32
African	Sub	1474	ACACACACACACACACACACACACACACA=1.0000	ACACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACACACA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	60	ACACACACACACACACACACACACACACA=1.00	ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1414	ACACACACACACACACACACACACACACA=1.0000	ACACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACACACACA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	86	ACACACACACACACACACACACACACACA=1.00	ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	70	ACACACACACACACACACACACACACACA=1.00	ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	ACACACACACACACACACACACACACACA=1.00	ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	96	ACACACACACACACACACACACACACACA=1.00	ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	516	ACACACACACACACACACACACACACACA=1.000	ACACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	78	ACACACACACACACACACACACACACACA=1.00	ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other	Sub	354	ACACACACACACACACACACACACACACA=0.997	ACACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.003, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACACACACA=0.000	0.99435	0.0	0.00565	0

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	14908	(AC)₁₄A=0.96619	del(CA)₇=0.00000, del(CA)₆=0.00000, del(CA)₅=0.00000, del(CA)₄=0.00000, del(CA)₃=0.00000, delCACA=0.00000, delCA=0.00054, dupCA=0.03320, dupCACA=0.00007, dup(CA)₃=0.00000, dup(CA)₄=0.00000, dup(CA)₅=0.00000, dup(CA)₆=0.00000, dup(CA)₇=0.00000
Allele Frequency Aggregator	European	Sub	12304	(AC)₁₄A=0.95912	del(CA)₇=0.00000, del(CA)₆=0.00000, del(CA)₅=0.00000, del(CA)₄=0.00000, del(CA)₃=0.00000, delCACA=0.00000, delCA=0.00065, dupCA=0.04015, dupCACA=0.00008, dup(CA)₃=0.00000, dup(CA)₄=0.00000, dup(CA)₅=0.00000, dup(CA)₆=0.00000, dup(CA)₇=0.00000
Allele Frequency Aggregator	African	Sub	1474	(AC)₁₄A=1.0000	del(CA)₇=0.0000, del(CA)₆=0.0000, del(CA)₅=0.0000, 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
Allele Frequency Aggregator	Latin American 2	Sub	516	(AC)₁₄A=1.000	del(CA)₇=0.000, del(CA)₆=0.000, del(CA)₅=0.000, 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
Allele Frequency Aggregator	Other	Sub	354	(AC)₁₄A=0.997	del(CA)₇=0.000, del(CA)₆=0.000, del(CA)₅=0.000, del(CA)₄=0.000, del(CA)₃=0.000, delCACA=0.000, delCA=0.000, dupCA=0.003, 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
Allele Frequency Aggregator	Latin American 1	Sub	96	(AC)₁₄A=1.00	del(CA)₇=0.00, del(CA)₆=0.00, del(CA)₅=0.00, 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
Allele Frequency Aggregator	Asian	Sub	86	(AC)₁₄A=1.00	del(CA)₇=0.00, del(CA)₆=0.00, del(CA)₅=0.00, 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
Allele Frequency Aggregator	South Asian	Sub	78	(AC)₁₄A=1.00	del(CA)₇=0.00, del(CA)₆=0.00, del(CA)₅=0.00, 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
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupCA=0.10

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 1	NC_000001.11:g.184911064CA[7]
GRCh38.p14 chr 1	NC_000001.11:g.184911064CA[8]
GRCh38.p14 chr 1	NC_000001.11:g.184911064CA[9]
GRCh38.p14 chr 1	NC_000001.11:g.184911064CA[10]
GRCh38.p14 chr 1	NC_000001.11:g.184911064CA[11]
GRCh38.p14 chr 1	NC_000001.11:g.184911064CA[12]
GRCh38.p14 chr 1	NC_000001.11:g.184911064CA[13]
GRCh38.p14 chr 1	NC_000001.11:g.184911064CA[15]
GRCh38.p14 chr 1	NC_000001.11:g.184911064CA[16]
GRCh38.p14 chr 1	NC_000001.11:g.184911064CA[17]
GRCh38.p14 chr 1	NC_000001.11:g.184911064CA[18]
GRCh38.p14 chr 1	NC_000001.11:g.184911064CA[19]
GRCh38.p14 chr 1	NC_000001.11:g.184911064CA[20]
GRCh38.p14 chr 1	NC_000001.11:g.184911064CA[21]
GRCh37.p13 chr 1	NC_000001.10:g.184880197CA[7]
GRCh37.p13 chr 1	NC_000001.10:g.184880197CA[8]
GRCh37.p13 chr 1	NC_000001.10:g.184880197CA[9]
GRCh37.p13 chr 1	NC_000001.10:g.184880197CA[10]
GRCh37.p13 chr 1	NC_000001.10:g.184880197CA[11]
GRCh37.p13 chr 1	NC_000001.10:g.184880197CA[12]
GRCh37.p13 chr 1	NC_000001.10:g.184880197CA[13]
GRCh37.p13 chr 1	NC_000001.10:g.184880197CA[15]
GRCh37.p13 chr 1	NC_000001.10:g.184880197CA[16]
GRCh37.p13 chr 1	NC_000001.10:g.184880197CA[17]
GRCh37.p13 chr 1	NC_000001.10:g.184880197CA[18]
GRCh37.p13 chr 1	NC_000001.10:g.184880197CA[19]
GRCh37.p13 chr 1	NC_000001.10:g.184880197CA[20]
GRCh37.p13 chr 1	NC_000001.10:g.184880197CA[21]
NIBAN1 RefSeqGene	NG_051588.1:g.68497GT[7]
NIBAN1 RefSeqGene	NG_051588.1:g.68497GT[8]
NIBAN1 RefSeqGene	NG_051588.1:g.68497GT[9]
NIBAN1 RefSeqGene	NG_051588.1:g.68497GT[10]
NIBAN1 RefSeqGene	NG_051588.1:g.68497GT[11]
NIBAN1 RefSeqGene	NG_051588.1:g.68497GT[12]
NIBAN1 RefSeqGene	NG_051588.1:g.68497GT[13]
NIBAN1 RefSeqGene	NG_051588.1:g.68497GT[15]
NIBAN1 RefSeqGene	NG_051588.1:g.68497GT[16]
NIBAN1 RefSeqGene	NG_051588.1:g.68497GT[17]
NIBAN1 RefSeqGene	NG_051588.1:g.68497GT[18]
NIBAN1 RefSeqGene	NG_051588.1:g.68497GT[19]
NIBAN1 RefSeqGene	NG_051588.1:g.68497GT[20]
NIBAN1 RefSeqGene	NG_051588.1:g.68497GT[21]

Gene: NIBAN1, niban apoptosis regulator 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NIBAN1 transcript	NM_052966.4:c.56-11781GT[… NM_052966.4:c.56-11781GT[7]	N/A	Intron Variant
NIBAN1 transcript variant X1	XM_047444091.1:c.233-1178… XM_047444091.1:c.233-11781GT[7]	N/A	Intron Variant
NIBAN1 transcript variant X2	XM_047444093.1:c.233-1178… XM_047444093.1:c.233-11781GT[7]	N/A	Intron Variant
NIBAN1 transcript variant X3	XM_047444094.1:c.233-1178… XM_047444094.1:c.233-11781GT[7]	N/A	Intron Variant
NIBAN1 transcript variant X4	XM_047444098.1:c.56-11781… XM_047444098.1:c.56-11781GT[7]	N/A	Intron Variant
NIBAN1 transcript variant X5	XM_047444102.1:c.56-11781… XM_047444102.1:c.56-11781GT[7]	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	(AC)₁₄A=	del(CA)₇	del(CA)₆	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
GRCh38.p14 chr 1	NC_000001.11:g.184911063_184911091=	NC_000001.11:g.184911064CA[7]	NC_000001.11:g.184911064CA[8]	NC_000001.11:g.184911064CA[9]	NC_000001.11:g.184911064CA[10]	NC_000001.11:g.184911064CA[11]	NC_000001.11:g.184911064CA[12]	NC_000001.11:g.184911064CA[13]	NC_000001.11:g.184911064CA[15]	NC_000001.11:g.184911064CA[16]	NC_000001.11:g.184911064CA[17]	NC_000001.11:g.184911064CA[18]	NC_000001.11:g.184911064CA[19]	NC_000001.11:g.184911064CA[20]	NC_000001.11:g.184911064CA[21]
GRCh37.p13 chr 1	NC_000001.10:g.184880196_184880224=	NC_000001.10:g.184880197CA[7]	NC_000001.10:g.184880197CA[8]	NC_000001.10:g.184880197CA[9]	NC_000001.10:g.184880197CA[10]	NC_000001.10:g.184880197CA[11]	NC_000001.10:g.184880197CA[12]	NC_000001.10:g.184880197CA[13]	NC_000001.10:g.184880197CA[15]	NC_000001.10:g.184880197CA[16]	NC_000001.10:g.184880197CA[17]	NC_000001.10:g.184880197CA[18]	NC_000001.10:g.184880197CA[19]	NC_000001.10:g.184880197CA[20]	NC_000001.10:g.184880197CA[21]
NIBAN1 RefSeqGene	NG_051588.1:g.68496_68524=	NG_051588.1:g.68497GT[7]	NG_051588.1:g.68497GT[8]	NG_051588.1:g.68497GT[9]	NG_051588.1:g.68497GT[10]	NG_051588.1:g.68497GT[11]	NG_051588.1:g.68497GT[12]	NG_051588.1:g.68497GT[13]	NG_051588.1:g.68497GT[15]	NG_051588.1:g.68497GT[16]	NG_051588.1:g.68497GT[17]	NG_051588.1:g.68497GT[18]	NG_051588.1:g.68497GT[19]	NG_051588.1:g.68497GT[20]	NG_051588.1:g.68497GT[21]
FAM129A transcript	NM_052966.3:c.56-11754=	NM_052966.3:c.56-11781GT[7]	NM_052966.3:c.56-11781GT[8]	NM_052966.3:c.56-11781GT[9]	NM_052966.3:c.56-11781GT[10]	NM_052966.3:c.56-11781GT[11]	NM_052966.3:c.56-11781GT[12]	NM_052966.3:c.56-11781GT[13]	NM_052966.3:c.56-11781GT[15]	NM_052966.3:c.56-11781GT[16]	NM_052966.3:c.56-11781GT[17]	NM_052966.3:c.56-11781GT[18]	NM_052966.3:c.56-11781GT[19]	NM_052966.3:c.56-11781GT[20]	NM_052966.3:c.56-11781GT[21]
NIBAN1 transcript	NM_052966.4:c.56-11754=	NM_052966.4:c.56-11781GT[7]	NM_052966.4:c.56-11781GT[8]	NM_052966.4:c.56-11781GT[9]	NM_052966.4:c.56-11781GT[10]	NM_052966.4:c.56-11781GT[11]	NM_052966.4:c.56-11781GT[12]	NM_052966.4:c.56-11781GT[13]	NM_052966.4:c.56-11781GT[15]	NM_052966.4:c.56-11781GT[16]	NM_052966.4:c.56-11781GT[17]	NM_052966.4:c.56-11781GT[18]	NM_052966.4:c.56-11781GT[19]	NM_052966.4:c.56-11781GT[20]	NM_052966.4:c.56-11781GT[21]
FAM129A transcript variant X1	XM_005244873.1:c.56-11754=	XM_005244873.1:c.56-11781GT[7]	XM_005244873.1:c.56-11781GT[8]	XM_005244873.1:c.56-11781GT[9]	XM_005244873.1:c.56-11781GT[10]	XM_005244873.1:c.56-11781GT[11]	XM_005244873.1:c.56-11781GT[12]	XM_005244873.1:c.56-11781GT[13]	XM_005244873.1:c.56-11781GT[15]	XM_005244873.1:c.56-11781GT[16]	XM_005244873.1:c.56-11781GT[17]	XM_005244873.1:c.56-11781GT[18]	XM_005244873.1:c.56-11781GT[19]	XM_005244873.1:c.56-11781GT[20]	XM_005244873.1:c.56-11781GT[21]
NIBAN1 transcript variant X1	XM_047444091.1:c.233-11754=	XM_047444091.1:c.233-11781GT[7]	XM_047444091.1:c.233-11781GT[8]	XM_047444091.1:c.233-11781GT[9]	XM_047444091.1:c.233-11781GT[10]	XM_047444091.1:c.233-11781GT[11]	XM_047444091.1:c.233-11781GT[12]	XM_047444091.1:c.233-11781GT[13]	XM_047444091.1:c.233-11781GT[15]	XM_047444091.1:c.233-11781GT[16]	XM_047444091.1:c.233-11781GT[17]	XM_047444091.1:c.233-11781GT[18]	XM_047444091.1:c.233-11781GT[19]	XM_047444091.1:c.233-11781GT[20]	XM_047444091.1:c.233-11781GT[21]
NIBAN1 transcript variant X2	XM_047444093.1:c.233-11754=	XM_047444093.1:c.233-11781GT[7]	XM_047444093.1:c.233-11781GT[8]	XM_047444093.1:c.233-11781GT[9]	XM_047444093.1:c.233-11781GT[10]	XM_047444093.1:c.233-11781GT[11]	XM_047444093.1:c.233-11781GT[12]	XM_047444093.1:c.233-11781GT[13]	XM_047444093.1:c.233-11781GT[15]	XM_047444093.1:c.233-11781GT[16]	XM_047444093.1:c.233-11781GT[17]	XM_047444093.1:c.233-11781GT[18]	XM_047444093.1:c.233-11781GT[19]	XM_047444093.1:c.233-11781GT[20]	XM_047444093.1:c.233-11781GT[21]
NIBAN1 transcript variant X3	XM_047444094.1:c.233-11754=	XM_047444094.1:c.233-11781GT[7]	XM_047444094.1:c.233-11781GT[8]	XM_047444094.1:c.233-11781GT[9]	XM_047444094.1:c.233-11781GT[10]	XM_047444094.1:c.233-11781GT[11]	XM_047444094.1:c.233-11781GT[12]	XM_047444094.1:c.233-11781GT[13]	XM_047444094.1:c.233-11781GT[15]	XM_047444094.1:c.233-11781GT[16]	XM_047444094.1:c.233-11781GT[17]	XM_047444094.1:c.233-11781GT[18]	XM_047444094.1:c.233-11781GT[19]	XM_047444094.1:c.233-11781GT[20]	XM_047444094.1:c.233-11781GT[21]
NIBAN1 transcript variant X4	XM_047444098.1:c.56-11754=	XM_047444098.1:c.56-11781GT[7]	XM_047444098.1:c.56-11781GT[8]	XM_047444098.1:c.56-11781GT[9]	XM_047444098.1:c.56-11781GT[10]	XM_047444098.1:c.56-11781GT[11]	XM_047444098.1:c.56-11781GT[12]	XM_047444098.1:c.56-11781GT[13]	XM_047444098.1:c.56-11781GT[15]	XM_047444098.1:c.56-11781GT[16]	XM_047444098.1:c.56-11781GT[17]	XM_047444098.1:c.56-11781GT[18]	XM_047444098.1:c.56-11781GT[19]	XM_047444098.1:c.56-11781GT[20]	XM_047444098.1:c.56-11781GT[21]
NIBAN1 transcript variant X5	XM_047444102.1:c.56-11754=	XM_047444102.1:c.56-11781GT[7]	XM_047444102.1:c.56-11781GT[8]	XM_047444102.1:c.56-11781GT[9]	XM_047444102.1:c.56-11781GT[10]	XM_047444102.1:c.56-11781GT[11]	XM_047444102.1:c.56-11781GT[12]	XM_047444102.1:c.56-11781GT[13]	XM_047444102.1:c.56-11781GT[15]	XM_047444102.1:c.56-11781GT[16]	XM_047444102.1:c.56-11781GT[17]	XM_047444102.1:c.56-11781GT[18]	XM_047444102.1:c.56-11781GT[19]	XM_047444102.1:c.56-11781GT[20]	XM_047444102.1:c.56-11781GT[21]

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#.

64 SubSNP, 36 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41221136	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss98579271	Oct 11, 2018 (152)
3	GMI	ss288064836	May 04, 2012 (137)
4	LUNTER	ss551023677	Apr 25, 2013 (138)
5	SSMP	ss663138873	Apr 01, 2015 (144)
6	1000GENOMES	ss1367921985	Aug 21, 2014 (142)
7	1000GENOMES	ss1367921986	Aug 21, 2014 (142)
8	1000GENOMES	ss1367921987	Aug 21, 2014 (142)
9	DDI	ss1536255942	Apr 01, 2015 (144)
10	EVA_GENOME_DK	ss1574061182	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1701513615	Jan 10, 2018 (151)
12	EVA_UK10K_TWINSUK	ss1701513619	Jan 10, 2018 (151)
13	EVA_UK10K_ALSPAC	ss1709960765	Oct 11, 2018 (152)
14	EVA_UK10K_TWINSUK	ss1709960775	Oct 11, 2018 (152)
15	SWEGEN	ss2988087891	Jan 10, 2018 (151)
16	MCHAISSO	ss3065338988	Nov 08, 2017 (151)
17	EVA_DECODE	ss3688189870	Jul 12, 2019 (153)
18	EVA_DECODE	ss3688189871	Jul 12, 2019 (153)
19	EVA_DECODE	ss3688189872	Jul 12, 2019 (153)
20	EVA_DECODE	ss3688189873	Jul 12, 2019 (153)
21	EVA_DECODE	ss3688189874	Jul 12, 2019 (153)
22	ACPOP	ss3727666695	Jul 12, 2019 (153)
23	ACPOP	ss3727666696	Jul 12, 2019 (153)
24	KHV_HUMAN_GENOMES	ss3800064652	Jul 12, 2019 (153)
25	EVA	ss3826532594	Apr 25, 2020 (154)
26	KOGIC	ss3946063136	Apr 25, 2020 (154)
27	KOGIC	ss3946063137	Apr 25, 2020 (154)
28	KOGIC	ss3946063138	Apr 25, 2020 (154)
29	GNOMAD	ss4007344713	Apr 25, 2021 (155)
30	GNOMAD	ss4007344714	Apr 25, 2021 (155)
31	GNOMAD	ss4007344715	Apr 25, 2021 (155)
32	GNOMAD	ss4007344716	Apr 25, 2021 (155)
33	GNOMAD	ss4007344717	Apr 25, 2021 (155)
34	GNOMAD	ss4007344718	Apr 25, 2021 (155)
35	GNOMAD	ss4007344719	Apr 25, 2021 (155)
36	GNOMAD	ss4007344720	Apr 25, 2021 (155)
37	GNOMAD	ss4007344721	Apr 25, 2021 (155)
38	GNOMAD	ss4007344722	Apr 25, 2021 (155)
39	GNOMAD	ss4007344723	Apr 25, 2021 (155)
40	TOPMED	ss4475682717	Apr 25, 2021 (155)
41	TOPMED	ss4475682718	Apr 25, 2021 (155)
42	TOPMED	ss4475682719	Apr 25, 2021 (155)
43	TOMMO_GENOMICS	ss5147424317	Apr 25, 2021 (155)
44	TOMMO_GENOMICS	ss5147424318	Apr 25, 2021 (155)
45	TOMMO_GENOMICS	ss5147424319	Apr 25, 2021 (155)
46	TOMMO_GENOMICS	ss5147424320	Apr 25, 2021 (155)
47	1000G_HIGH_COVERAGE	ss5245017047	Oct 12, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5245017048	Oct 12, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5245017049	Oct 12, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5245017050	Oct 12, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5245017051	Oct 12, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5245017052	Oct 12, 2022 (156)
53	HUGCELL_USP	ss5445530190	Oct 12, 2022 (156)
54	HUGCELL_USP	ss5445530191	Oct 12, 2022 (156)
55	HUGCELL_USP	ss5445530192	Oct 12, 2022 (156)
56	HUGCELL_USP	ss5445530193	Oct 12, 2022 (156)
57	HUGCELL_USP	ss5445530194	Oct 12, 2022 (156)
58	TOMMO_GENOMICS	ss5674895121	Oct 12, 2022 (156)
59	TOMMO_GENOMICS	ss5674895122	Oct 12, 2022 (156)
60	TOMMO_GENOMICS	ss5674895123	Oct 12, 2022 (156)
61	TOMMO_GENOMICS	ss5674895124	Oct 12, 2022 (156)
62	EVA	ss5832952421	Oct 12, 2022 (156)
63	EVA	ss5832952422	Oct 12, 2022 (156)
64	EVA	ss5849191312	Oct 12, 2022 (156)
65	1000Genomes Submission ignored due to conflicting rows: Row 4584571 (NC_000001.10:184880195::AC 684/5008) Row 4584572 (NC_000001.10:184880195::ACAC 123/5008) Row 4584573 (NC_000001.10:184880195::ACACAC 11/5008)	-	Oct 11, 2018 (152)
66	1000Genomes Submission ignored due to conflicting rows: Row 4584571 (NC_000001.10:184880195::AC 684/5008) Row 4584572 (NC_000001.10:184880195::ACAC 123/5008) Row 4584573 (NC_000001.10:184880195::ACACAC 11/5008)	-	Oct 11, 2018 (152)
67	1000Genomes Submission ignored due to conflicting rows: Row 4584571 (NC_000001.10:184880195::AC 684/5008) Row 4584572 (NC_000001.10:184880195::ACAC 123/5008) Row 4584573 (NC_000001.10:184880195::ACACAC 11/5008)	-	Oct 11, 2018 (152)
68	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 2515097 (NC_000001.10:184880195::AC 490/3854) Row 2515098 (NC_000001.10:184880195:AC: 150/3854)	-	Oct 11, 2018 (152)
69	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 2515097 (NC_000001.10:184880195::AC 490/3854) Row 2515098 (NC_000001.10:184880195:AC: 150/3854)	-	Oct 11, 2018 (152)
70	The Danish reference pan genome	NC_000001.10 - 184880196	Apr 25, 2020 (154)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33080062 (NC_000001.11:184911062::AC 18793/132746) Row 33080063 (NC_000001.11:184911062::ACAC 3201/132834) Row 33080064 (NC_000001.11:184911062::ACACAC 509/132854)...	-	Apr 25, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33080062 (NC_000001.11:184911062::AC 18793/132746) Row 33080063 (NC_000001.11:184911062::ACAC 3201/132834) Row 33080064 (NC_000001.11:184911062::ACACAC 509/132854)...	-	Apr 25, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33080062 (NC_000001.11:184911062::AC 18793/132746) Row 33080063 (NC_000001.11:184911062::ACAC 3201/132834) Row 33080064 (NC_000001.11:184911062::ACACAC 509/132854)...	-	Apr 25, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33080062 (NC_000001.11:184911062::AC 18793/132746) Row 33080063 (NC_000001.11:184911062::ACAC 3201/132834) Row 33080064 (NC_000001.11:184911062::ACACAC 509/132854)...	-	Apr 25, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33080062 (NC_000001.11:184911062::AC 18793/132746) Row 33080063 (NC_000001.11:184911062::ACAC 3201/132834) Row 33080064 (NC_000001.11:184911062::ACACAC 509/132854)...	-	Apr 25, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33080062 (NC_000001.11:184911062::AC 18793/132746) Row 33080063 (NC_000001.11:184911062::ACAC 3201/132834) Row 33080064 (NC_000001.11:184911062::ACACAC 509/132854)...	-	Apr 25, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33080062 (NC_000001.11:184911062::AC 18793/132746) Row 33080063 (NC_000001.11:184911062::ACAC 3201/132834) Row 33080064 (NC_000001.11:184911062::ACACAC 509/132854)...	-	Apr 25, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33080062 (NC_000001.11:184911062::AC 18793/132746) Row 33080063 (NC_000001.11:184911062::ACAC 3201/132834) Row 33080064 (NC_000001.11:184911062::ACACAC 509/132854)...	-	Apr 25, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33080062 (NC_000001.11:184911062::AC 18793/132746) Row 33080063 (NC_000001.11:184911062::ACAC 3201/132834) Row 33080064 (NC_000001.11:184911062::ACACAC 509/132854)...	-	Apr 25, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33080062 (NC_000001.11:184911062::AC 18793/132746) Row 33080063 (NC_000001.11:184911062::ACAC 3201/132834) Row 33080064 (NC_000001.11:184911062::ACACAC 509/132854)...	-	Apr 25, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33080062 (NC_000001.11:184911062::AC 18793/132746) Row 33080063 (NC_000001.11:184911062::ACAC 3201/132834) Row 33080064 (NC_000001.11:184911062::ACACAC 509/132854)...	-	Apr 25, 2021 (155)
82	Korean Genome Project Submission ignored due to conflicting rows: Row 2441137 (NC_000001.11:184911064::AC 250/1832) Row 2441138 (NC_000001.11:184911062:AC: 35/1832) Row 2441139 (NC_000001.11:184911064::ACAC 12/1832)	-	Apr 25, 2020 (154)
83	Korean Genome Project Submission ignored due to conflicting rows: Row 2441137 (NC_000001.11:184911064::AC 250/1832) Row 2441138 (NC_000001.11:184911062:AC: 35/1832) Row 2441139 (NC_000001.11:184911064::ACAC 12/1832)	-	Apr 25, 2020 (154)
84	Korean Genome Project Submission ignored due to conflicting rows: Row 2441137 (NC_000001.11:184911064::AC 250/1832) Row 2441138 (NC_000001.11:184911062:AC: 35/1832) Row 2441139 (NC_000001.11:184911064::ACAC 12/1832)	-	Apr 25, 2020 (154)
85	Northern Sweden Submission ignored due to conflicting rows: Row 951560 (NC_000001.10:184880195::AC 49/600) Row 951561 (NC_000001.10:184880195:AC: 3/600)	-	Jul 12, 2019 (153)
86	Northern Sweden Submission ignored due to conflicting rows: Row 951560 (NC_000001.10:184880195::AC 49/600) Row 951561 (NC_000001.10:184880195:AC: 3/600)	-	Jul 12, 2019 (153)
87	8.3KJPN Submission ignored due to conflicting rows: Row 5393624 (NC_000001.10:184880195::ACAC 130/16760) Row 5393625 (NC_000001.10:184880195::AC 2196/16760) Row 5393626 (NC_000001.10:184880195:AC: 44/16760)...	-	Apr 25, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 5393624 (NC_000001.10:184880195::ACAC 130/16760) Row 5393625 (NC_000001.10:184880195::AC 2196/16760) Row 5393626 (NC_000001.10:184880195:AC: 44/16760)...	-	Apr 25, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 5393624 (NC_000001.10:184880195::ACAC 130/16760) Row 5393625 (NC_000001.10:184880195::AC 2196/16760) Row 5393626 (NC_000001.10:184880195:AC: 44/16760)...	-	Apr 25, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 5393624 (NC_000001.10:184880195::ACAC 130/16760) Row 5393625 (NC_000001.10:184880195::AC 2196/16760) Row 5393626 (NC_000001.10:184880195:AC: 44/16760)...	-	Apr 25, 2021 (155)
91	14KJPN Submission ignored due to conflicting rows: Row 8732225 (NC_000001.11:184911062::AC 3615/28256) Row 8732226 (NC_000001.11:184911062:AC: 53/28256) Row 8732227 (NC_000001.11:184911062::ACAC 228/28256)...	-	Oct 12, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 8732225 (NC_000001.11:184911062::AC 3615/28256) Row 8732226 (NC_000001.11:184911062:AC: 53/28256) Row 8732227 (NC_000001.11:184911062::ACAC 228/28256)...	-	Oct 12, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 8732225 (NC_000001.11:184911062::AC 3615/28256) Row 8732226 (NC_000001.11:184911062:AC: 53/28256) Row 8732227 (NC_000001.11:184911062::ACAC 228/28256)...	-	Oct 12, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 8732225 (NC_000001.11:184911062::AC 3615/28256) Row 8732226 (NC_000001.11:184911062:AC: 53/28256) Row 8732227 (NC_000001.11:184911062::ACAC 228/28256)...	-	Oct 12, 2022 (156)
95	TopMed Submission ignored due to conflicting rows: Row 39289052 (NC_000001.11:184911062::ACAC 6660/264690) Row 39289053 (NC_000001.11:184911062:ACAC: 316/264690) Row 39289054 (NC_000001.11:184911062:ACACACACACACAC: 1/264690)	-	Apr 25, 2021 (155)
96	TopMed Submission ignored due to conflicting rows: Row 39289052 (NC_000001.11:184911062::ACAC 6660/264690) Row 39289053 (NC_000001.11:184911062:ACAC: 316/264690) Row 39289054 (NC_000001.11:184911062:ACACACACACACAC: 1/264690)	-	Apr 25, 2021 (155)
97	TopMed Submission ignored due to conflicting rows: Row 39289052 (NC_000001.11:184911062::ACAC 6660/264690) Row 39289053 (NC_000001.11:184911062:ACAC: 316/264690) Row 39289054 (NC_000001.11:184911062:ACACACACACACAC: 1/264690)	-	Apr 25, 2021 (155)
98	UK 10K study - Twins Submission ignored due to conflicting rows: Row 2515097 (NC_000001.10:184880195::AC 486/3708) Row 2515098 (NC_000001.10:184880195:AC: 142/3708)	-	Oct 11, 2018 (152)
99	UK 10K study - Twins Submission ignored due to conflicting rows: Row 2515097 (NC_000001.10:184880195::AC 486/3708) Row 2515098 (NC_000001.10:184880195:AC: 142/3708)	-	Oct 11, 2018 (152)
100	ALFA	NC_000001.11 - 184911063	Apr 25, 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)
rs371333841	May 15, 2013 (138)
rs796570627	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4475682719	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACAC:	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACA	(self)
9100724477	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACA	(self)
ss4007344723	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACAC:	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACA	(self)
9100724477	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACA	(self)
ss4007344722	NC_000001.11:184911062:ACACACACAC:	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACA	(self)
9100724477	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACA	(self)
ss3688189874, ss4007344721	NC_000001.11:184911062:ACACACAC:	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
9100724477	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss4007344720	NC_000001.11:184911062:ACACAC:	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
9100724477	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss5147424320	NC_000001.10:184880195:ACAC:	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss4007344719, ss4475682718, ss5245017051, ss5445530194, ss5674895124	NC_000001.11:184911062:ACAC:	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
9100724477	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss3688189873	NC_000001.11:184911066:ACAC:	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss1701513615, ss1701513619, ss2988087891, ss3727666696, ss5147424319, ss5832952422	NC_000001.10:184880195:AC:	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss3946063137, ss4007344718, ss5245017052, ss5445530191, ss5674895122	NC_000001.11:184911062:AC:	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
9100724477	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss3688189872	NC_000001.11:184911068:AC:	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss551023677	NC_000001.9:183146818::AC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss288064836	NC_000001.9:183146847::CA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
185854, ss663138873, ss1367921985, ss1536255942, ss1574061182, ss3727666695, ss3826532594, ss5147424318, ss5832952421	NC_000001.10:184880195::AC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss1709960765, ss1709960775	NC_000001.10:184880197::AC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss3065338988, ss3800064652, ss4007344713, ss5245017047, ss5445530190, ss5674895121, ss5849191312	NC_000001.11:184911062::AC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
9100724477	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss3946063136	NC_000001.11:184911064::AC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss3688189871	NC_000001.11:184911070::AC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss41221136	NT_004487.19:36368837::AC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss98579271	NT_004487.19:36368866::CA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss1367921986, ss5147424317	NC_000001.10:184880195::ACAC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	(self)
ss4007344714, ss4475682717, ss5245017049, ss5445530192, ss5674895123	NC_000001.11:184911062::ACAC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	(self)
9100724477	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	(self)
ss3946063138	NC_000001.11:184911064::ACAC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	(self)
ss3688189870	NC_000001.11:184911070::ACAC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	(self)
ss1367921987	NC_000001.10:184880195::ACACAC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	(self)
ss4007344715, ss5245017050, ss5445530193	NC_000001.11:184911062::ACACAC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	(self)
9100724477	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	(self)
ss4007344716, ss5245017048	NC_000001.11:184911062::ACACACAC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA	(self)
9100724477	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA	(self)
ss4007344717	NC_000001.11:184911062::ACACACACAC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACA	(self)
9100724477	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACA	(self)
9100724477	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACA	(self)
9100724477	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACA	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3097570608	NC_000001.11:184911062::ACACACACAC… NC_000001.11:184911062::ACACACACACAC	NC_000001.11:184911062:ACACACACACA… NC_000001.11:184911062:ACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACA

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

No publications for rs35550596

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

rs35550596