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rs876658220

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658220(-;-)
Make rs876658220(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position21971147
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs876658220
ebirs876658220
HLIrs876658220
Exacrs876658220
Varsomers876658220
Maprs876658220
PheGenIrs876658220
hapmaprs876658220
1000 genomesrs876658220
hgdprs876658220
ensemblrs876658220
gopubmedrs876658220
geneviewrs876658220
scholarrs876658220
googlers876658220
pharmgkbrs876658220
gwascentralrs876658220
openSNPrs876658220
23andMers876658220
23andMe allrs876658220
SNP Nexus

SNPshotrs876658220
SNPdbers876658220
MSV3drs876658220
GWAS Ctlgrs876658220
Max Magnitude0
ClinVar
Risk rs876658220(;)
Alt rs876658220(;)
Reference rs876658220(A;A)
Significance Probable-Pathogenic
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.21971146delT
CLNSRC
CLNACC RCV000214923.1,