Name: rs58572396
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.

rs58572396

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr18:31398027-31398049 (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)₁₄ / del(A)₁₂ / del(A)₁₁ / d…
del(A)₁₄ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / ins(A)₂₆
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₄=0.000 (0/980, ALFA)
del(A)₁₂=0.000 (0/980, ALFA)
del(A)₁₁=0.000 (0/980, ALFA) (+ 9 more)
del(A)₁₀=0.000 (0/980, ALFA)
del(A)₉=0.000 (0/980, ALFA)
del(A)₈=0.000 (0/980, ALFA)
del(A)₆=0.000 (0/980, ALFA)
del(A)₄=0.000 (0/980, ALFA)
delAAA=0.000 (0/980, ALFA)
delAA=0.000 (0/980, ALFA)
delA=0.000 (0/980, ALFA)
dupA=0.000 (0/980, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DSG1-AS1 : Intron Variant
DSG4 : 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	980	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	812	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	102	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	4	AAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	98	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	8	AAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	14	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	8	AAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	32	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	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	980	(A)₂₃=1.000	del(A)₁₄=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	European	Sub	812	(A)₂₃=1.000	del(A)₁₄=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	African	Sub	102	(A)₂₃=1.000	del(A)₁₄=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	Other	Sub	32	(A)₂₃=1.00	del(A)₁₄=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Latin American 2	Sub	14	(A)₂₃=1.00	del(A)₁₄=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	8	(A)₂₃=1.0	del(A)₁₄=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₆=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	South Asian	Sub	8	(A)₂₃=1.0	del(A)₁₄=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₆=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	Asian	Sub	4	(A)₂₃=1.0	del(A)₁₄=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₆=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=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 18	NC_000018.10:g.31398036_31398049del
GRCh38.p14 chr 18	NC_000018.10:g.31398038_31398049del
GRCh38.p14 chr 18	NC_000018.10:g.31398039_31398049del
GRCh38.p14 chr 18	NC_000018.10:g.31398040_31398049del
GRCh38.p14 chr 18	NC_000018.10:g.31398041_31398049del
GRCh38.p14 chr 18	NC_000018.10:g.31398042_31398049del
GRCh38.p14 chr 18	NC_000018.10:g.31398043_31398049del
GRCh38.p14 chr 18	NC_000018.10:g.31398044_31398049del
GRCh38.p14 chr 18	NC_000018.10:g.31398046_31398049del
GRCh38.p14 chr 18	NC_000018.10:g.31398047_31398049del
GRCh38.p14 chr 18	NC_000018.10:g.31398048_31398049del
GRCh38.p14 chr 18	NC_000018.10:g.31398049del
GRCh38.p14 chr 18	NC_000018.10:g.31398049dup
GRCh38.p14 chr 18	NC_000018.10:g.31398048_31398049dup
GRCh38.p14 chr 18	NC_000018.10:g.31398047_31398049dup
GRCh38.p14 chr 18	NC_000018.10:g.31398046_31398049dup
GRCh38.p14 chr 18	NC_000018.10:g.31398045_31398049dup
GRCh38.p14 chr 18	NC_000018.10:g.31398044_31398049dup
GRCh38.p14 chr 18	NC_000018.10:g.31398043_31398049dup
GRCh38.p14 chr 18	NC_000018.10:g.31398049_31398050insAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 18	NC_000018.9:g.28977999_28978012del
GRCh37.p13 chr 18	NC_000018.9:g.28978001_28978012del
GRCh37.p13 chr 18	NC_000018.9:g.28978002_28978012del
GRCh37.p13 chr 18	NC_000018.9:g.28978003_28978012del
GRCh37.p13 chr 18	NC_000018.9:g.28978004_28978012del
GRCh37.p13 chr 18	NC_000018.9:g.28978005_28978012del
GRCh37.p13 chr 18	NC_000018.9:g.28978006_28978012del
GRCh37.p13 chr 18	NC_000018.9:g.28978007_28978012del
GRCh37.p13 chr 18	NC_000018.9:g.28978009_28978012del
GRCh37.p13 chr 18	NC_000018.9:g.28978010_28978012del
GRCh37.p13 chr 18	NC_000018.9:g.28978011_28978012del
GRCh37.p13 chr 18	NC_000018.9:g.28978012del
GRCh37.p13 chr 18	NC_000018.9:g.28978012dup
GRCh37.p13 chr 18	NC_000018.9:g.28978011_28978012dup
GRCh37.p13 chr 18	NC_000018.9:g.28978010_28978012dup
GRCh37.p13 chr 18	NC_000018.9:g.28978009_28978012dup
GRCh37.p13 chr 18	NC_000018.9:g.28978008_28978012dup
GRCh37.p13 chr 18	NC_000018.9:g.28978007_28978012dup
GRCh37.p13 chr 18	NC_000018.9:g.28978006_28978012dup
GRCh37.p13 chr 18	NC_000018.9:g.28978012_28978013insAAAAAAAAAAAAAAAAAAAAAAAAAA
DSG4 RefSeqGene	NG_013040.1:g.26260_26273del
DSG4 RefSeqGene	NG_013040.1:g.26262_26273del
DSG4 RefSeqGene	NG_013040.1:g.26263_26273del
DSG4 RefSeqGene	NG_013040.1:g.26264_26273del
DSG4 RefSeqGene	NG_013040.1:g.26265_26273del
DSG4 RefSeqGene	NG_013040.1:g.26266_26273del
DSG4 RefSeqGene	NG_013040.1:g.26267_26273del
DSG4 RefSeqGene	NG_013040.1:g.26268_26273del
DSG4 RefSeqGene	NG_013040.1:g.26270_26273del
DSG4 RefSeqGene	NG_013040.1:g.26271_26273del
DSG4 RefSeqGene	NG_013040.1:g.26272_26273del
DSG4 RefSeqGene	NG_013040.1:g.26273del
DSG4 RefSeqGene	NG_013040.1:g.26273dup
DSG4 RefSeqGene	NG_013040.1:g.26272_26273dup
DSG4 RefSeqGene	NG_013040.1:g.26271_26273dup
DSG4 RefSeqGene	NG_013040.1:g.26270_26273dup
DSG4 RefSeqGene	NG_013040.1:g.26269_26273dup
DSG4 RefSeqGene	NG_013040.1:g.26268_26273dup
DSG4 RefSeqGene	NG_013040.1:g.26267_26273dup
DSG4 RefSeqGene	NG_013040.1:g.26273_26274insAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: DSG4, desmoglein 4 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DSG4 transcript variant 1	NM_001134453.3:c.1006-123… NM_001134453.3:c.1006-1236_1006-1223del	N/A	Intron Variant
DSG4 transcript variant 2	NM_177986.5:c.1006-1236_1… NM_177986.5:c.1006-1236_1006-1223del	N/A	Intron Variant

Gene: DSG1-AS1, DSG1 antisense RNA 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DSG1-AS1 transcript variant 1	NR_110788.1:n.	N/A	Intron Variant
DSG1-AS1 transcript variant 2	NR_110789.1:n.	N/A	Genic Upstream Transcript 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)₂₃=	del(A)₁₄	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	ins(A)₂₆
GRCh38.p14 chr 18	NC_000018.10:g.31398027_31398049=	NC_000018.10:g.31398036_31398049del	NC_000018.10:g.31398038_31398049del	NC_000018.10:g.31398039_31398049del	NC_000018.10:g.31398040_31398049del	NC_000018.10:g.31398041_31398049del	NC_000018.10:g.31398042_31398049del	NC_000018.10:g.31398043_31398049del	NC_000018.10:g.31398044_31398049del	NC_000018.10:g.31398046_31398049del	NC_000018.10:g.31398047_31398049del	NC_000018.10:g.31398048_31398049del	NC_000018.10:g.31398049del	NC_000018.10:g.31398049dup	NC_000018.10:g.31398048_31398049dup	NC_000018.10:g.31398047_31398049dup	NC_000018.10:g.31398046_31398049dup	NC_000018.10:g.31398045_31398049dup	NC_000018.10:g.31398044_31398049dup	NC_000018.10:g.31398043_31398049dup	NC_000018.10:g.31398049_31398050insAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 18	NC_000018.9:g.28977990_28978012=	NC_000018.9:g.28977999_28978012del	NC_000018.9:g.28978001_28978012del	NC_000018.9:g.28978002_28978012del	NC_000018.9:g.28978003_28978012del	NC_000018.9:g.28978004_28978012del	NC_000018.9:g.28978005_28978012del	NC_000018.9:g.28978006_28978012del	NC_000018.9:g.28978007_28978012del	NC_000018.9:g.28978009_28978012del	NC_000018.9:g.28978010_28978012del	NC_000018.9:g.28978011_28978012del	NC_000018.9:g.28978012del	NC_000018.9:g.28978012dup	NC_000018.9:g.28978011_28978012dup	NC_000018.9:g.28978010_28978012dup	NC_000018.9:g.28978009_28978012dup	NC_000018.9:g.28978008_28978012dup	NC_000018.9:g.28978007_28978012dup	NC_000018.9:g.28978006_28978012dup	NC_000018.9:g.28978012_28978013insAAAAAAAAAAAAAAAAAAAAAAAAAA
DSG4 RefSeqGene	NG_013040.1:g.26251_26273=	NG_013040.1:g.26260_26273del	NG_013040.1:g.26262_26273del	NG_013040.1:g.26263_26273del	NG_013040.1:g.26264_26273del	NG_013040.1:g.26265_26273del	NG_013040.1:g.26266_26273del	NG_013040.1:g.26267_26273del	NG_013040.1:g.26268_26273del	NG_013040.1:g.26270_26273del	NG_013040.1:g.26271_26273del	NG_013040.1:g.26272_26273del	NG_013040.1:g.26273del	NG_013040.1:g.26273dup	NG_013040.1:g.26272_26273dup	NG_013040.1:g.26271_26273dup	NG_013040.1:g.26270_26273dup	NG_013040.1:g.26269_26273dup	NG_013040.1:g.26268_26273dup	NG_013040.1:g.26267_26273dup	NG_013040.1:g.26273_26274insAAAAAAAAAAAAAAAAAAAAAAAAAA
DSG4 transcript variant 1	NM_001134453.1:c.1006-1245=	NM_001134453.1:c.1006-1236_1006-1223del	NM_001134453.1:c.1006-1234_1006-1223del	NM_001134453.1:c.1006-1233_1006-1223del	NM_001134453.1:c.1006-1232_1006-1223del	NM_001134453.1:c.1006-1231_1006-1223del	NM_001134453.1:c.1006-1230_1006-1223del	NM_001134453.1:c.1006-1229_1006-1223del	NM_001134453.1:c.1006-1228_1006-1223del	NM_001134453.1:c.1006-1226_1006-1223del	NM_001134453.1:c.1006-1225_1006-1223del	NM_001134453.1:c.1006-1224_1006-1223del	NM_001134453.1:c.1006-1223del	NM_001134453.1:c.1006-1223dup	NM_001134453.1:c.1006-1224_1006-1223dup	NM_001134453.1:c.1006-1225_1006-1223dup	NM_001134453.1:c.1006-1226_1006-1223dup	NM_001134453.1:c.1006-1227_1006-1223dup	NM_001134453.1:c.1006-1228_1006-1223dup	NM_001134453.1:c.1006-1229_1006-1223dup	NM_001134453.1:c.1006-1223_1006-1222insAAAAAAAAAAAAAAAAAAAAAAAAAA
DSG4 transcript variant 1	NM_001134453.3:c.1006-1245=	NM_001134453.3:c.1006-1236_1006-1223del	NM_001134453.3:c.1006-1234_1006-1223del	NM_001134453.3:c.1006-1233_1006-1223del	NM_001134453.3:c.1006-1232_1006-1223del	NM_001134453.3:c.1006-1231_1006-1223del	NM_001134453.3:c.1006-1230_1006-1223del	NM_001134453.3:c.1006-1229_1006-1223del	NM_001134453.3:c.1006-1228_1006-1223del	NM_001134453.3:c.1006-1226_1006-1223del	NM_001134453.3:c.1006-1225_1006-1223del	NM_001134453.3:c.1006-1224_1006-1223del	NM_001134453.3:c.1006-1223del	NM_001134453.3:c.1006-1223dup	NM_001134453.3:c.1006-1224_1006-1223dup	NM_001134453.3:c.1006-1225_1006-1223dup	NM_001134453.3:c.1006-1226_1006-1223dup	NM_001134453.3:c.1006-1227_1006-1223dup	NM_001134453.3:c.1006-1228_1006-1223dup	NM_001134453.3:c.1006-1229_1006-1223dup	NM_001134453.3:c.1006-1223_1006-1222insAAAAAAAAAAAAAAAAAAAAAAAAAA
DSG4 transcript variant 2	NM_177986.3:c.1006-1245=	NM_177986.3:c.1006-1236_1006-1223del	NM_177986.3:c.1006-1234_1006-1223del	NM_177986.3:c.1006-1233_1006-1223del	NM_177986.3:c.1006-1232_1006-1223del	NM_177986.3:c.1006-1231_1006-1223del	NM_177986.3:c.1006-1230_1006-1223del	NM_177986.3:c.1006-1229_1006-1223del	NM_177986.3:c.1006-1228_1006-1223del	NM_177986.3:c.1006-1226_1006-1223del	NM_177986.3:c.1006-1225_1006-1223del	NM_177986.3:c.1006-1224_1006-1223del	NM_177986.3:c.1006-1223del	NM_177986.3:c.1006-1223dup	NM_177986.3:c.1006-1224_1006-1223dup	NM_177986.3:c.1006-1225_1006-1223dup	NM_177986.3:c.1006-1226_1006-1223dup	NM_177986.3:c.1006-1227_1006-1223dup	NM_177986.3:c.1006-1228_1006-1223dup	NM_177986.3:c.1006-1229_1006-1223dup	NM_177986.3:c.1006-1223_1006-1222insAAAAAAAAAAAAAAAAAAAAAAAAAA
DSG4 transcript variant 2	NM_177986.5:c.1006-1245=	NM_177986.5:c.1006-1236_1006-1223del	NM_177986.5:c.1006-1234_1006-1223del	NM_177986.5:c.1006-1233_1006-1223del	NM_177986.5:c.1006-1232_1006-1223del	NM_177986.5:c.1006-1231_1006-1223del	NM_177986.5:c.1006-1230_1006-1223del	NM_177986.5:c.1006-1229_1006-1223del	NM_177986.5:c.1006-1228_1006-1223del	NM_177986.5:c.1006-1226_1006-1223del	NM_177986.5:c.1006-1225_1006-1223del	NM_177986.5:c.1006-1224_1006-1223del	NM_177986.5:c.1006-1223del	NM_177986.5:c.1006-1223dup	NM_177986.5:c.1006-1224_1006-1223dup	NM_177986.5:c.1006-1225_1006-1223dup	NM_177986.5:c.1006-1226_1006-1223dup	NM_177986.5:c.1006-1227_1006-1223dup	NM_177986.5:c.1006-1228_1006-1223dup	NM_177986.5:c.1006-1229_1006-1223dup	NM_177986.5:c.1006-1223_1006-1222insAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

42 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80085602	Dec 15, 2007 (129)
2	HGSV	ss80475901	Dec 15, 2007 (129)
3	HGSV	ss82554720	Dec 15, 2007 (129)
4	HGSV	ss82748579	Dec 15, 2007 (129)
5	SWEGEN	ss3016347666	Nov 08, 2017 (151)
6	URBANLAB	ss3650768943	Oct 12, 2018 (152)
7	EVA_DECODE	ss3701440410	Jul 13, 2019 (153)
8	EVA_DECODE	ss3701440411	Jul 13, 2019 (153)
9	EVA_DECODE	ss3701440412	Jul 13, 2019 (153)
10	EVA_DECODE	ss3701440413	Jul 13, 2019 (153)
11	EVA_DECODE	ss3701440414	Jul 13, 2019 (153)
12	EVA	ss3835114714	Apr 27, 2020 (154)
13	GNOMAD	ss4320023641	Apr 27, 2021 (155)
14	GNOMAD	ss4320023642	Apr 27, 2021 (155)
15	GNOMAD	ss4320023643	Apr 27, 2021 (155)
16	GNOMAD	ss4320023644	Apr 27, 2021 (155)
17	GNOMAD	ss4320023645	Apr 27, 2021 (155)
18	GNOMAD	ss4320023646	Apr 27, 2021 (155)
19	GNOMAD	ss4320023647	Apr 27, 2021 (155)
20	GNOMAD	ss4320023648	Apr 27, 2021 (155)
21	GNOMAD	ss4320023650	Apr 27, 2021 (155)
22	GNOMAD	ss4320023651	Apr 27, 2021 (155)
23	GNOMAD	ss4320023652	Apr 27, 2021 (155)
24	GNOMAD	ss4320023653	Apr 27, 2021 (155)
25	GNOMAD	ss4320023654	Apr 27, 2021 (155)
26	GNOMAD	ss4320023655	Apr 27, 2021 (155)
27	GNOMAD	ss4320023656	Apr 27, 2021 (155)
28	TOMMO_GENOMICS	ss5224666167	Apr 27, 2021 (155)
29	TOMMO_GENOMICS	ss5224666168	Apr 27, 2021 (155)
30	TOMMO_GENOMICS	ss5224666169	Apr 27, 2021 (155)
31	1000G_HIGH_COVERAGE	ss5304900498	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5304900499	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5304900501	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5497710103	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5497710104	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5497710105	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5497710106	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5497710107	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5497710108	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5782312682	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5782312683	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5782312684	Oct 16, 2022 (156)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 521196528 (NC_000018.10:31398026::A 321/73856) Row 521196529 (NC_000018.10:31398026::AA 73/74068) Row 521196530 (NC_000018.10:31398026::AAA 6/74182)...	-	Apr 27, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 82635474 (NC_000018.9:28977989:A: 13059/16456) Row 82635475 (NC_000018.9:28977989:AA: 22/16456) Row 82635476 (NC_000018.9:28977989::A 70/16456)	-	Apr 27, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 82635474 (NC_000018.9:28977989:A: 13059/16456) Row 82635475 (NC_000018.9:28977989:AA: 22/16456) Row 82635476 (NC_000018.9:28977989::A 70/16456)	-	Apr 27, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 82635474 (NC_000018.9:28977989:A: 13059/16456) Row 82635475 (NC_000018.9:28977989:AA: 22/16456) Row 82635476 (NC_000018.9:28977989::A 70/16456)	-	Apr 27, 2021 (155)
62	14KJPN Submission ignored due to conflicting rows: Row 116149786 (NC_000018.10:31398026:A: 23620/28176) Row 116149787 (NC_000018.10:31398026:AA: 29/28176) Row 116149788 (NC_000018.10:31398026::A 126/28176)	-	Oct 16, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 116149786 (NC_000018.10:31398026:A: 23620/28176) Row 116149787 (NC_000018.10:31398026:AA: 29/28176) Row 116149788 (NC_000018.10:31398026::A 126/28176)	-	Oct 16, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 116149786 (NC_000018.10:31398026:A: 23620/28176) Row 116149787 (NC_000018.10:31398026:AA: 29/28176) Row 116149788 (NC_000018.10:31398026::A 126/28176)	-	Oct 16, 2022 (156)
65	ALFA	NC_000018.10 - 31398027	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs71959171	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
12390941087	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
12390941087	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
12390941087	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4320023656	NC_000018.10:31398026:AAAAAAAAAA:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
12390941087	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4320023655	NC_000018.10:31398026:AAAAAAAAA:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
12390941087	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4320023654, ss5497710108	NC_000018.10:31398026:AAAAAAAA:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
12390941087	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4320023653	NC_000018.10:31398026:AAAAAAA:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
12390941087	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3701440414, ss4320023652	NC_000018.10:31398026:AAAA:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
12390941087	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4320023651, ss5304900501, ss5497710107	NC_000018.10:31398026:AAA:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
12390941087	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3701440413	NC_000018.10:31398027:AAA:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss80085602	NC_000018.8:27232008:AA:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3016347666, ss5224666168	NC_000018.9:28977989:AA:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4320023650, ss5304900499, ss5497710106, ss5782312683	NC_000018.10:31398026:AA:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
12390941087	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3701440412	NC_000018.10:31398028:AA:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss80475901, ss82554720, ss82748579	NC_000018.8:27232009:A:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3835114714, ss5224666167	NC_000018.9:28977989:A:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3650768943, ss5497710103, ss5782312682	NC_000018.10:31398026:A:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
12390941087	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3701440411	NC_000018.10:31398029:A:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5224666169	NC_000018.9:28977989::A	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4320023641, ss5304900498, ss5497710104, ss5782312684	NC_000018.10:31398026::A	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
12390941087	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3701440410	NC_000018.10:31398030::A	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4320023642, ss5497710105	NC_000018.10:31398026::AA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4320023643	NC_000018.10:31398026::AAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4320023644	NC_000018.10:31398026::AAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4320023645	NC_000018.10:31398026::AAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4320023646	NC_000018.10:31398026::AAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4320023647	NC_000018.10:31398026::AAAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4320023648	NC_000018.10:31398026::AAAAAAAAAAA… NC_000018.10:31398026::AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3276302864	NC_000018.10:31398026:AAAAAA:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA
ss3276302867	NC_000018.10:31398026:AAAAAAAAAAAA:	NC_000018.10:31398026:AAAAAAAAAAAA… NC_000018.10:31398026:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA

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

No publications for rs58572396

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

rs58572396