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rs876660860

From SNPedia

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Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs876660860(GA;T)
Make rs876660860(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position36996676
GeneMLH1
is asnp
is mentioned by
dbSNPrs876660860
ebirs876660860
HLIrs876660860
Exacrs876660860
Varsomers876660860
Maprs876660860
PheGenIrs876660860
hapmaprs876660860
1000 genomesrs876660860
hgdprs876660860
ensemblrs876660860
gopubmedrs876660860
geneviewrs876660860
scholarrs876660860
googlers876660860
pharmgkbrs876660860
gwascentralrs876660860
openSNPrs876660860
23andMers876660860
23andMe allrs876660860
SNP Nexus

SNPshotrs876660860
SNPdbers876660860
MSV3drs876660860
GWAS Ctlgrs876660860
Max Magnitude0
ClinVar
Risk rs876660860(T;T)
Alt rs876660860(T;T)
Reference rs876660860(GA;GA)
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.37038167_37038168delGAinsT
CLNSRC
CLNACC RCV000215802.1,