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rs876660214

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876660214(-;-)
Make rs876660214(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37020343
GeneMLH1
is asnp
is mentioned by
dbSNPrs876660214
ebirs876660214
HLIrs876660214
Exacrs876660214
Varsomers876660214
Maprs876660214
PheGenIrs876660214
hapmaprs876660214
1000 genomesrs876660214
hgdprs876660214
ensemblrs876660214
gopubmedrs876660214
geneviewrs876660214
scholarrs876660214
googlers876660214
pharmgkbrs876660214
gwascentralrs876660214
openSNPrs876660214
23andMers876660214
23andMe allrs876660214
SNP Nexus

SNPshotrs876660214
SNPdbers876660214
MSV3drs876660214
GWAS Ctlgrs876660214
Max Magnitude0
ClinVar
Risk rs876660214(;)
Alt rs876660214(;)
Reference rs876660214(T;T)
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.37061834delT
CLNSRC
CLNACC RCV000223113.1,