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rs876660943

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660943(G;T)
Make rs876660943(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47806359
GeneMSH6
is asnp
is mentioned by
dbSNPrs876660943
ebirs876660943
HLIrs876660943
Exacrs876660943
Varsomers876660943
Maprs876660943
PheGenIrs876660943
hapmaprs876660943
1000 genomesrs876660943
hgdprs876660943
ensemblrs876660943
gopubmedrs876660943
geneviewrs876660943
scholarrs876660943
googlers876660943
pharmgkbrs876660943
gwascentralrs876660943
openSNPrs876660943
23andMers876660943
23andMe allrs876660943
SNP Nexus

SNPshotrs876660943
SNPdbers876660943
MSV3drs876660943
GWAS Ctlgrs876660943
Max Magnitude0
ClinVar
Risk rs876660943(T;T)
Alt rs876660943(T;T)
Reference rs876660943(G;G)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Lynch syndrome
Variation info
Gene MSH6
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033498G>T
CLNSRC
CLNACC RCV000217114.1, RCV000226322.1,