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rs730881677

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881677(C;C)
Make rs730881677(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position21971209
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs730881677
ebirs730881677
HLIrs730881677
Exacrs730881677
Varsomers730881677
Maprs730881677
PheGenIrs730881677
hapmaprs730881677
1000 genomesrs730881677
hgdprs730881677
ensemblrs730881677
gopubmedrs730881677
geneviewrs730881677
scholarrs730881677
googlers730881677
pharmgkbrs730881677
gwascentralrs730881677
openSNPrs730881677
23andMers730881677
23andMe allrs730881677
SNP Nexus

SNPshotrs730881677
SNPdbers730881677
MSV3drs730881677
GWAS Ctlgrs730881677
Max Magnitude0
ClinVar
Risk rs730881677(C;C)
Alt rs730881677(C;C)
Reference rs730881677(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CDKN2A
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000009.11:g.21971208C>G
CLNSRC
CLNACC RCV000160412.1, RCV000222665.1,