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rs63750764

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750764(-;-)
Make rs63750764(-;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37014447
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750764
ebirs63750764
HLIrs63750764
Exacrs63750764
Varsomers63750764
Maprs63750764
PheGenIrs63750764
hapmaprs63750764
1000 genomesrs63750764
hgdprs63750764
ensemblrs63750764
gopubmedrs63750764
geneviewrs63750764
scholarrs63750764
googlers63750764
pharmgkbrs63750764
gwascentralrs63750764
openSNPrs63750764
23andMers63750764
23andMe allrs63750764
SNP Nexus

SNPshotrs63750764
SNPdbers63750764
MSV3drs63750764
GWAS Ctlgrs63750764
Max Magnitude0
ClinVar
Risk rs63750764(;)
Alt rs63750764(;)
Reference rs63750764(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37055938delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075825.2,