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rs63750760

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750760(C;T)
Make rs63750760(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025751
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750760
ebirs63750760
HLIrs63750760
Exacrs63750760
Varsomers63750760
Maprs63750760
PheGenIrs63750760
hapmaprs63750760
1000 genomesrs63750760
hgdprs63750760
ensemblrs63750760
gopubmedrs63750760
geneviewrs63750760
scholarrs63750760
googlers63750760
pharmgkbrs63750760
gwascentralrs63750760
openSNPrs63750760
23andMers63750760
23andMe allrs63750760
SNP Nexus

SNPshotrs63750760
SNPdbers63750760
MSV3drs63750760
GWAS Ctlgrs63750760
Max Magnitude0
ClinVar
Risk rs63750760(T;T)
Alt rs63750760(T;T)
Reference rs63750760(C;C)
Significance Probable-Pathogenic
Disease Lynch syndrome not specified Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Lynch syndrome not specified Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37067242C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075124.2, RCV000202088.1, RCV000217569.2,