Name: rs9306769
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.

rs9306769

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chrX:23784569-23784588 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₀ / del(T)₈ / del(T)₆ / del…
del(T)₁₀ / del(T)₈ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.1444 (926/6414, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SAT1 : Intron Variant
LOC105373148 : 2KB Upstream 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	6414	TTTTTTTTTTTTTTTTTTTT=0.6632	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0147, TTTTTTTTTTTTTTTTTTTTTTT=0.1225, TTTTTTTTTTTTTTTTTTTTTTTT=0.0447, TTTTTTTTTTTTTTTTTTTTTT=0.1444, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0078, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0027	0.837718	0.140429	0.021854	32
European	Sub	5456	TTTTTTTTTTTTTTTTTTTT=0.6041	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0172, TTTTTTTTTTTTTTTTTTTTTTT=0.1441, TTTTTTTTTTTTTTTTTTTTTTTT=0.0526, TTTTTTTTTTTTTTTTTTTTTT=0.1697, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0092, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0031	0.798695	0.174197	0.027108	32
African	Sub	604	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	18	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	586	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	20	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	14	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	6	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	42	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	178	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	12	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	102	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6414	(T)₂₀=0.6632	del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0147, dupTT=0.1444, dupTTT=0.1225, dup(T)₄=0.0447, dup(T)₅=0.0078, dup(T)₆=0.0027
Allele Frequency Aggregator	European	Sub	5456	(T)₂₀=0.6041	del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0172, dupTT=0.1697, dupTTT=0.1441, dup(T)₄=0.0526, dup(T)₅=0.0092, dup(T)₆=0.0031
Allele Frequency Aggregator	African	Sub	604	(T)₂₀=1.000	del(T)₁₀=0.000, del(T)₈=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	178	(T)₂₀=1.000	del(T)₁₀=0.000, del(T)₈=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Other	Sub	102	(T)₂₀=1.000	del(T)₁₀=0.000, del(T)₈=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	42	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₈=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Asian	Sub	20	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₈=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	12	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₈=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00

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 X	NC_000023.11:g.23784579_23784588del
GRCh38.p14 chr X	NC_000023.11:g.23784581_23784588del
GRCh38.p14 chr X	NC_000023.11:g.23784583_23784588del
GRCh38.p14 chr X	NC_000023.11:g.23784584_23784588del
GRCh38.p14 chr X	NC_000023.11:g.23784585_23784588del
GRCh38.p14 chr X	NC_000023.11:g.23784586_23784588del
GRCh38.p14 chr X	NC_000023.11:g.23784587_23784588del
GRCh38.p14 chr X	NC_000023.11:g.23784588del
GRCh38.p14 chr X	NC_000023.11:g.23784588dup
GRCh38.p14 chr X	NC_000023.11:g.23784587_23784588dup
GRCh38.p14 chr X	NC_000023.11:g.23784586_23784588dup
GRCh38.p14 chr X	NC_000023.11:g.23784585_23784588dup
GRCh38.p14 chr X	NC_000023.11:g.23784584_23784588dup
GRCh38.p14 chr X	NC_000023.11:g.23784583_23784588dup
GRCh38.p14 chr X	NC_000023.11:g.23784582_23784588dup
GRCh38.p14 chr X	NC_000023.11:g.23784581_23784588dup
GRCh38.p14 chr X	NC_000023.11:g.23784580_23784588dup
GRCh38.p14 chr X	NC_000023.11:g.23784579_23784588dup
GRCh37.p13 chr X	NC_000023.10:g.23802696_23802705del
GRCh37.p13 chr X	NC_000023.10:g.23802698_23802705del
GRCh37.p13 chr X	NC_000023.10:g.23802700_23802705del
GRCh37.p13 chr X	NC_000023.10:g.23802701_23802705del
GRCh37.p13 chr X	NC_000023.10:g.23802702_23802705del
GRCh37.p13 chr X	NC_000023.10:g.23802703_23802705del
GRCh37.p13 chr X	NC_000023.10:g.23802704_23802705del
GRCh37.p13 chr X	NC_000023.10:g.23802705del
GRCh37.p13 chr X	NC_000023.10:g.23802705dup
GRCh37.p13 chr X	NC_000023.10:g.23802704_23802705dup
GRCh37.p13 chr X	NC_000023.10:g.23802703_23802705dup
GRCh37.p13 chr X	NC_000023.10:g.23802702_23802705dup
GRCh37.p13 chr X	NC_000023.10:g.23802701_23802705dup
GRCh37.p13 chr X	NC_000023.10:g.23802700_23802705dup
GRCh37.p13 chr X	NC_000023.10:g.23802699_23802705dup
GRCh37.p13 chr X	NC_000023.10:g.23802698_23802705dup
GRCh37.p13 chr X	NC_000023.10:g.23802697_23802705dup
GRCh37.p13 chr X	NC_000023.10:g.23802696_23802705dup
SAT1 RefSeqGene	NG_012929.1:g.6422_6431del
SAT1 RefSeqGene	NG_012929.1:g.6424_6431del
SAT1 RefSeqGene	NG_012929.1:g.6426_6431del
SAT1 RefSeqGene	NG_012929.1:g.6427_6431del
SAT1 RefSeqGene	NG_012929.1:g.6428_6431del
SAT1 RefSeqGene	NG_012929.1:g.6429_6431del
SAT1 RefSeqGene	NG_012929.1:g.6430_6431del
SAT1 RefSeqGene	NG_012929.1:g.6431del
SAT1 RefSeqGene	NG_012929.1:g.6431dup
SAT1 RefSeqGene	NG_012929.1:g.6430_6431dup
SAT1 RefSeqGene	NG_012929.1:g.6429_6431dup
SAT1 RefSeqGene	NG_012929.1:g.6428_6431dup
SAT1 RefSeqGene	NG_012929.1:g.6427_6431dup
SAT1 RefSeqGene	NG_012929.1:g.6426_6431dup
SAT1 RefSeqGene	NG_012929.1:g.6425_6431dup
SAT1 RefSeqGene	NG_012929.1:g.6424_6431dup
SAT1 RefSeqGene	NG_012929.1:g.6423_6431dup
SAT1 RefSeqGene	NG_012929.1:g.6422_6431dup

Gene: SAT1, spermidine/spermine N1-acetyltransferase 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SAT1 transcript variant 1	NM_002970.4:c.202+696_202… NM_002970.4:c.202+696_202+705del	N/A	Intron Variant
SAT1 transcript variant 2	NR_027783.3:n.	N/A	Intron Variant
SAT1 transcript variant X1	XM_047442338.1:c.	N/A	Genic Upstream Transcript Variant

Gene: LOC105373148, uncharacterized LOC105373148 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105373148 transcript variant X1	XR_001755813.2:n.	N/A	Upstream Transcript Variant
LOC105373148 transcript variant X5	XR_001755814.2:n.	N/A	Upstream Transcript Variant
LOC105373148 transcript variant X6	XR_001755816.3:n.	N/A	Upstream Transcript Variant
LOC105373148 transcript variant X3	XR_001755817.2:n.	N/A	Upstream Transcript Variant
LOC105373148 transcript variant X7	XR_007068413.1:n.	N/A	Upstream Transcript Variant
LOC105373148 transcript variant X2	XR_950535.3:n.	N/A	Upstream Transcript Variant
LOC105373148 transcript variant X4	XR_001755815.2:n.	N/A	N/A

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₀=	del(T)₁₀	del(T)₈	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀
GRCh38.p14 chr X	NC_000023.11:g.23784569_23784588=	NC_000023.11:g.23784579_23784588del	NC_000023.11:g.23784581_23784588del	NC_000023.11:g.23784583_23784588del	NC_000023.11:g.23784584_23784588del	NC_000023.11:g.23784585_23784588del	NC_000023.11:g.23784586_23784588del	NC_000023.11:g.23784587_23784588del	NC_000023.11:g.23784588del	NC_000023.11:g.23784588dup	NC_000023.11:g.23784587_23784588dup	NC_000023.11:g.23784586_23784588dup	NC_000023.11:g.23784585_23784588dup	NC_000023.11:g.23784584_23784588dup	NC_000023.11:g.23784583_23784588dup	NC_000023.11:g.23784582_23784588dup	NC_000023.11:g.23784581_23784588dup	NC_000023.11:g.23784580_23784588dup	NC_000023.11:g.23784579_23784588dup
GRCh37.p13 chr X	NC_000023.10:g.23802686_23802705=	NC_000023.10:g.23802696_23802705del	NC_000023.10:g.23802698_23802705del	NC_000023.10:g.23802700_23802705del	NC_000023.10:g.23802701_23802705del	NC_000023.10:g.23802702_23802705del	NC_000023.10:g.23802703_23802705del	NC_000023.10:g.23802704_23802705del	NC_000023.10:g.23802705del	NC_000023.10:g.23802705dup	NC_000023.10:g.23802704_23802705dup	NC_000023.10:g.23802703_23802705dup	NC_000023.10:g.23802702_23802705dup	NC_000023.10:g.23802701_23802705dup	NC_000023.10:g.23802700_23802705dup	NC_000023.10:g.23802699_23802705dup	NC_000023.10:g.23802698_23802705dup	NC_000023.10:g.23802697_23802705dup	NC_000023.10:g.23802696_23802705dup
SAT1 RefSeqGene	NG_012929.1:g.6412_6431=	NG_012929.1:g.6422_6431del	NG_012929.1:g.6424_6431del	NG_012929.1:g.6426_6431del	NG_012929.1:g.6427_6431del	NG_012929.1:g.6428_6431del	NG_012929.1:g.6429_6431del	NG_012929.1:g.6430_6431del	NG_012929.1:g.6431del	NG_012929.1:g.6431dup	NG_012929.1:g.6430_6431dup	NG_012929.1:g.6429_6431dup	NG_012929.1:g.6428_6431dup	NG_012929.1:g.6427_6431dup	NG_012929.1:g.6426_6431dup	NG_012929.1:g.6425_6431dup	NG_012929.1:g.6424_6431dup	NG_012929.1:g.6423_6431dup	NG_012929.1:g.6422_6431dup
SAT1 transcript variant 1	NM_002970.2:c.202+686=	NM_002970.2:c.202+696_202+705del	NM_002970.2:c.202+698_202+705del	NM_002970.2:c.202+700_202+705del	NM_002970.2:c.202+701_202+705del	NM_002970.2:c.202+702_202+705del	NM_002970.2:c.202+703_202+705del	NM_002970.2:c.202+704_202+705del	NM_002970.2:c.202+705del	NM_002970.2:c.202+705dup	NM_002970.2:c.202+704_202+705dup	NM_002970.2:c.202+703_202+705dup	NM_002970.2:c.202+702_202+705dup	NM_002970.2:c.202+701_202+705dup	NM_002970.2:c.202+700_202+705dup	NM_002970.2:c.202+699_202+705dup	NM_002970.2:c.202+698_202+705dup	NM_002970.2:c.202+697_202+705dup	NM_002970.2:c.202+696_202+705dup
SAT1 transcript variant 1	NM_002970.4:c.202+686=	NM_002970.4:c.202+696_202+705del	NM_002970.4:c.202+698_202+705del	NM_002970.4:c.202+700_202+705del	NM_002970.4:c.202+701_202+705del	NM_002970.4:c.202+702_202+705del	NM_002970.4:c.202+703_202+705del	NM_002970.4:c.202+704_202+705del	NM_002970.4:c.202+705del	NM_002970.4:c.202+705dup	NM_002970.4:c.202+704_202+705dup	NM_002970.4:c.202+703_202+705dup	NM_002970.4:c.202+702_202+705dup	NM_002970.4:c.202+701_202+705dup	NM_002970.4:c.202+700_202+705dup	NM_002970.4:c.202+699_202+705dup	NM_002970.4:c.202+698_202+705dup	NM_002970.4:c.202+697_202+705dup	NM_002970.4:c.202+696_202+705dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

52 SubSNP, 35 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81873515	Dec 14, 2007 (130)
2	PJP	ss295448585	Oct 12, 2018 (152)
3	EVA_UK10K_ALSPAC	ss1709677492	Apr 01, 2015 (144)
4	EVA_UK10K_ALSPAC	ss1709677494	Apr 01, 2015 (144)
5	EVA_UK10K_TWINSUK	ss1709677578	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1709677579	Apr 01, 2015 (144)
7	SWEGEN	ss3019736756	Nov 08, 2017 (151)
8	SWEGEN	ss3019736757	Nov 08, 2017 (151)
9	SWEGEN	ss3019736758	Nov 08, 2017 (151)
10	SWEGEN	ss3019736759	Nov 08, 2017 (151)
11	MCHAISSO	ss3065257113	Nov 08, 2017 (151)
12	EVA	ss3836117244	Apr 27, 2020 (154)
13	GNOMAD	ss4369030027	Apr 26, 2021 (155)
14	GNOMAD	ss4369030028	Apr 26, 2021 (155)
15	GNOMAD	ss4369030029	Apr 26, 2021 (155)
16	GNOMAD	ss4369030030	Apr 26, 2021 (155)
17	GNOMAD	ss4369030031	Apr 26, 2021 (155)
18	GNOMAD	ss4369030032	Apr 26, 2021 (155)
19	GNOMAD	ss4369030033	Apr 26, 2021 (155)
20	GNOMAD	ss4369030034	Apr 26, 2021 (155)
21	GNOMAD	ss4369030035	Apr 26, 2021 (155)
22	GNOMAD	ss4369030036	Apr 26, 2021 (155)
23	GNOMAD	ss4369030038	Apr 26, 2021 (155)
24	GNOMAD	ss4369030039	Apr 26, 2021 (155)
25	GNOMAD	ss4369030040	Apr 26, 2021 (155)
26	GNOMAD	ss4369030041	Apr 26, 2021 (155)
27	GNOMAD	ss4369030042	Apr 26, 2021 (155)
28	GNOMAD	ss4369030043	Apr 26, 2021 (155)
29	GNOMAD	ss4369030044	Apr 26, 2021 (155)
30	GNOMAD	ss4369030045	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5233832326	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5233832327	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5233832328	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5233832329	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5233832330	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5233832331	Apr 26, 2021 (155)
37	1000G_HIGH_COVERAGE	ss5312038018	Oct 16, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5312038019	Oct 16, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5312038020	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5312038021	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5312038022	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5312038023	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5503760351	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5503760352	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5503760353	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5503760354	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5795349769	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5795349770	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5795349771	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5795349772	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5795349773	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5795349774	Oct 16, 2022 (156)
53	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 45175098 (NC_000023.10:23802685::TT 2252/2889) Row 45175099 (NC_000023.10:23802685::TTT 637/2889)	-	Oct 12, 2018 (152)
54	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 45175098 (NC_000023.10:23802685::TT 2252/2889) Row 45175099 (NC_000023.10:23802685::TTT 637/2889)	-	Oct 12, 2018 (152)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576941736 (NC_000023.11:23784568::T 2277/57445) Row 576941737 (NC_000023.11:23784568::TT 17985/57370) Row 576941738 (NC_000023.11:23784568::TTT 17942/57220)...	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 91801633 (NC_000023.10:23802685::TTT 2158/11707) Row 91801634 (NC_000023.10:23802685::TT 4564/11707) Row 91801635 (NC_000023.10:23802685:T: 28/11707)...	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 91801633 (NC_000023.10:23802685::TTT 2158/11707) Row 91801634 (NC_000023.10:23802685::TT 4564/11707) Row 91801635 (NC_000023.10:23802685:T: 28/11707)...	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 91801633 (NC_000023.10:23802685::TTT 2158/11707) Row 91801634 (NC_000023.10:23802685::TT 4564/11707) Row 91801635 (NC_000023.10:23802685:T: 28/11707)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 91801633 (NC_000023.10:23802685::TTT 2158/11707) Row 91801634 (NC_000023.10:23802685::TT 4564/11707) Row 91801635 (NC_000023.10:23802685:T: 28/11707)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 91801633 (NC_000023.10:23802685::TTT 2158/11707) Row 91801634 (NC_000023.10:23802685::TT 4564/11707) Row 91801635 (NC_000023.10:23802685:T: 28/11707)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 91801633 (NC_000023.10:23802685::TTT 2158/11707) Row 91801634 (NC_000023.10:23802685::TT 4564/11707) Row 91801635 (NC_000023.10:23802685:T: 28/11707)...	-	Apr 26, 2021 (155)
79	14KJPN Submission ignored due to conflicting rows: Row 129186873 (NC_000023.11:23784568::TT 9434/21979) Row 129186874 (NC_000023.11:23784568::TTT 4374/21979) Row 129186875 (NC_000023.11:23784568:T: 63/21979)...	-	Oct 16, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 129186873 (NC_000023.11:23784568::TT 9434/21979) Row 129186874 (NC_000023.11:23784568::TTT 4374/21979) Row 129186875 (NC_000023.11:23784568:T: 63/21979)...	-	Oct 16, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 129186873 (NC_000023.11:23784568::TT 9434/21979) Row 129186874 (NC_000023.11:23784568::TTT 4374/21979) Row 129186875 (NC_000023.11:23784568:T: 63/21979)...	-	Oct 16, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 129186873 (NC_000023.11:23784568::TT 9434/21979) Row 129186874 (NC_000023.11:23784568::TTT 4374/21979) Row 129186875 (NC_000023.11:23784568:T: 63/21979)...	-	Oct 16, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 129186873 (NC_000023.11:23784568::TT 9434/21979) Row 129186874 (NC_000023.11:23784568::TTT 4374/21979) Row 129186875 (NC_000023.11:23784568:T: 63/21979)...	-	Oct 16, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 129186873 (NC_000023.11:23784568::TT 9434/21979) Row 129186874 (NC_000023.11:23784568::TTT 4374/21979) Row 129186875 (NC_000023.11:23784568:T: 63/21979)...	-	Oct 16, 2022 (156)
85	UK 10K study - Twins Submission ignored due to conflicting rows: Row 45175098 (NC_000023.10:23802685::TT 2612/3708) Row 45175099 (NC_000023.10:23802685::TTT 1096/3708)	-	Oct 12, 2018 (152)
86	UK 10K study - Twins Submission ignored due to conflicting rows: Row 45175098 (NC_000023.10:23802685::TT 2612/3708) Row 45175099 (NC_000023.10:23802685::TTT 1096/3708)	-	Oct 12, 2018 (152)
87	ALFA	NC_000023.11 - 23784569	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)
rs58166480	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4369030045	NC_000023.11:23784568:TTTTTTTTTT:	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
2506680080	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss5233832330	NC_000023.10:23802685:TTTTTTTT:	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4369030044, ss5795349773	NC_000023.11:23784568:TTTTTTTT:	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
2506680080	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4369030043	NC_000023.11:23784568:TTTTTT:	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
2506680080	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4369030042	NC_000023.11:23784568:TTTTT:	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
2506680080	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4369030041	NC_000023.11:23784568:TTTT:	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
2506680080	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4369030040	NC_000023.11:23784568:TTT:	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
2506680080	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4369030039	NC_000023.11:23784568:TT:	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
2506680080	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5233832328	NC_000023.10:23802685:T:	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4369030038, ss5312038019, ss5795349771	NC_000023.11:23784568:T:	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
2506680080	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3019736759, ss5233832329	NC_000023.10:23802685::T	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4369030027, ss5312038018, ss5503760353, ss5795349772	NC_000023.11:23784568::T	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
2506680080	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss1709677492, ss1709677578, ss3019736756, ss5233832327	NC_000023.10:23802685::TT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3065257113, ss4369030028, ss5312038020, ss5503760354, ss5795349769	NC_000023.11:23784568::TT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
2506680080	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss81873515	NT_167197.1:21684467::TT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss295448585	NC_000023.9:23712607::TTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1709677494, ss1709677579, ss3019736757, ss3836117244, ss5233832326	NC_000023.10:23802685::TTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4369030029, ss5312038021, ss5503760351, ss5795349770	NC_000023.11:23784568::TTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
2506680080	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3019736758, ss5233832331	NC_000023.10:23802685::TTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4369030030, ss5312038022, ss5503760352, ss5795349774	NC_000023.11:23784568::TTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
2506680080	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4369030031, ss5312038023	NC_000023.11:23784568::TTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2506680080	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4369030032	NC_000023.11:23784568::TTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2506680080	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4369030033	NC_000023.11:23784568::TTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4369030034	NC_000023.11:23784568::TTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4369030035	NC_000023.11:23784568::TTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4369030036	NC_000023.11:23784568::TTTTTTTTTT	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2486664608	NC_000023.10:23802685:TTTTTTTTTT:	NC_000023.11:23784568:TTTTTTTTTTTT… NC_000023.11:23784568:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT

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

No publications for rs9306769

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

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

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs9306769