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

rs63750610

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750610(C;T)
Make rs63750610(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048563
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750610
ebirs63750610
HLIrs63750610
Exacrs63750610
Varsomers63750610
Maprs63750610
PheGenIrs63750610
hapmaprs63750610
1000 genomesrs63750610
hgdprs63750610
ensemblrs63750610
gopubmedrs63750610
geneviewrs63750610
scholarrs63750610
googlers63750610
pharmgkbrs63750610
gwascentralrs63750610
openSNPrs63750610
23andMers63750610
23andMe allrs63750610
SNP Nexus

SNPshotrs63750610
SNPdbers63750610
MSV3drs63750610
GWAS Ctlgrs63750610
Max Magnitude0
ClinVar
Risk rs63750610(T;T)
Alt rs63750610(T;T)
Reference rs63750610(C;C)
Significance Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37090054C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075433.2, RCV000221413.1,