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rs137854598

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854598(A;A)
Make rs137854598(A;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position21971054
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs137854598
ebirs137854598
HLIrs137854598
Exacrs137854598
Varsomers137854598
Maprs137854598
PheGenIrs137854598
hapmaprs137854598
1000 genomesrs137854598
hgdprs137854598
ensemblrs137854598
gopubmedrs137854598
geneviewrs137854598
scholarrs137854598
googlers137854598
pharmgkbrs137854598
gwascentralrs137854598
openSNPrs137854598
23andMers137854598
23andMe allrs137854598
SNP Nexus

SNPshotrs137854598
SNPdbers137854598
MSV3drs137854598
GWAS Ctlgrs137854598
Max Magnitude0
OMIM600160
Desc
Variant0011
Relatedalso
ClinVar
Risk rs137854598(A,T;A,T)
Alt rs137854598(A,T;A,T)
Reference rs137854598(C;C)
Significance Untested
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CDKN2A
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000009.11:g.21971053G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000220450.1,