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rs876660822

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660822(-;-)
Make rs876660822(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37000999
GeneMLH1
is asnp
is mentioned by
dbSNPrs876660822
ebirs876660822
HLIrs876660822
Exacrs876660822
Varsomers876660822
Maprs876660822
PheGenIrs876660822
hapmaprs876660822
1000 genomesrs876660822
hgdprs876660822
ensemblrs876660822
gopubmedrs876660822
geneviewrs876660822
scholarrs876660822
googlers876660822
pharmgkbrs876660822
gwascentralrs876660822
openSNPrs876660822
23andMers876660822
23andMe allrs876660822
SNP Nexus

SNPshotrs876660822
SNPdbers876660822
MSV3drs876660822
GWAS Ctlgrs876660822
Max Magnitude0
ClinVar
Risk rs876660822(;)
Alt rs876660822(;)
Reference rs876660822(A;A)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37042490delA
CLNSRC
CLNACC RCV000214057.1,