Have questions? Visit https://www.reddit.com/r/SNPedia

rs876659681

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659681(-;-)
Make rs876659681(-;TT)
Make rs876659681(TT;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37048984
GeneMLH1
is asnp
is mentioned by
dbSNPrs876659681
ebirs876659681
HLIrs876659681
Exacrs876659681
Varsomers876659681
Maprs876659681
PheGenIrs876659681
hapmaprs876659681
1000 genomesrs876659681
hgdprs876659681
ensemblrs876659681
gopubmedrs876659681
geneviewrs876659681
scholarrs876659681
googlers876659681
pharmgkbrs876659681
gwascentralrs876659681
openSNPrs876659681
23andMers876659681
23andMe allrs876659681
SNP Nexus

SNPshotrs876659681
SNPdbers876659681
MSV3drs876659681
GWAS Ctlgrs876659681
Max Magnitude0
ClinVar
Risk rs876659681(TT;TT)
Alt rs876659681(TT;TT)
Reference rs876659681(;)
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.37090475_37090476insTT
CLNSRC
CLNACC RCV000221270.1,