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dbSNP Short Genetic Variations

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.


Current Build 151

Released July 17, 2018

Homo sapiens
chr11:32391968 (GRCh38.p7) 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.

Variation Type
SNV Single Nucleotide Variation
Clinical Significance
Reported in ClinVar
Gene : Consequence
WT1 : Intron Variant
10 citations
Genomic View
See rs on genome

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.p7 chr 11 NC_000011.10:g.32391968G>A
GRCh37.p13 chr 11 NC_000011.9:g.32413514G>A
WT1 RefSeqGene (LRG_525) NG_009272.1:g.48574C>T
Gene: WT1, Wilms tumor 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
WT1 transcript variant A NM_000378.4:c. N/A Intron Variant
WT1 transcript variant E NM_001198551.1:c. N/A Intron Variant
WT1 transcript variant F NM_001198552.1:c. N/A Intron Variant
WT1 transcript variant B NM_024424.3:c. N/A Intron Variant
WT1 transcript variant D NM_024426.4:c. 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.

Allele: A (allele ID: 18539 )
ClinVar Accession Disease Names Clinical Significance
RCV000003674.2 Frasier syndrome Pathogenic
RCV000003675.2 Diffuse mesangial sclerosis Pathogenic
RCV000157584.1 Hereditary nephrotic syndrome Pathogenic
RCV000489749.1 not provided Pathogenic

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").


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 G= A Note
GRCh38.p7 chr 11 NC_000011.10:g.32391968G= NC_000011.10:g.32391968G>A
GRCh37.p13 chr 11 NC_000011.9:g.32413514G= NC_000011.9:g.32413514G>A
WT1 RefSeqGene (LRG_525) NG_009272.1:g.48574C= NG_009272.1:g.48574C>T

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#.

2 SubSNP, 4 ClinVar submissions
No Submitter Submission ID Date (Build)
1 OMIM-CURATED-RECORDS ss1399966073 Jul 27, 2016 (147)
2 OMIM-CURATED-RECORDS ss1399967384 Oct 16, 2014 (142)
3 ClinVar RCV000003674.2 Jul 20, 2018 (151)
4 ClinVar RCV000003675.2 Jul 20, 2018 (151)
5 ClinVar RCV000157584.1 Jul 20, 2018 (151)
6 ClinVar RCV000489749.1 Jul 20, 2018 (151)

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).

Added to this RefSNP Cluster:
Submission ids Observation SPDI Canonical SPDI Source RSIDs
ss1399966073, ss1399967384 NC_000011.10:32391967:G= NC_000011.10:32391967:G= (self)
RCV000003674.2, RCV000003675.2, RCV000157584.1, RCV000489749.1, ss1399966073, ss1399967384 NC_000011.10:32391967:G>A NC_000011.10:32391967:G>A (self)

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

10 citations for rs587776577
PMID Title Author Year Journal
1658787 Alternative splicing and genomic structure of the Wilms tumor gene WT1. Haber DA et al. 1991 Proceedings of the National Academy of Sciences of the United States of America
9398852 Donor splice-site mutations in WT1 are responsible for Frasier syndrome. Barbaux S et al. 1997 Nature genetics
9499425 Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms. Klamt B et al. 1998 Human molecular genetics
9529364 Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database. Jeanpierre C et al. 1998 American journal of human genetics
10094551 The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor. Barbosa AS et al. 1999 Human mutation
12050205 An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis. Melo KF et al. 2002 The Journal of clinical endocrinology and metabolism
19484379 Single gene disorders. 2008 Genomic medicine
20442690 WT1 gene mutations in Chinese children with early onset nephrotic syndrome. Li J et al. 2010 Pediatric research
23515051 Genetic screening in adolescents with steroid-resistant nephrotic syndrome. Lipska BS et al. 2013 Kidney international
24161391 Two distinct WT1 mutations identified in patients and relatives with isolated nephrotic proteinuria. Guaragna MS et al. 2013 Biochemical and biophysical research communications

Genomic regions, transcripts, and products
Top Help

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

Software version is: 0.1.4.post833+d3ba21e