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rs63750641

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750641(A;G)
Make rs63750641(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37000997
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750641
ebirs63750641
HLIrs63750641
Exacrs63750641
Varsomers63750641
Maprs63750641
PheGenIrs63750641
hapmaprs63750641
1000 genomesrs63750641
hgdprs63750641
ensemblrs63750641
gopubmedrs63750641
geneviewrs63750641
scholarrs63750641
googlers63750641
pharmgkbrs63750641
gwascentralrs63750641
openSNPrs63750641
23andMers63750641
23andMe allrs63750641
SNP Nexus

SNPshotrs63750641
SNPdbers63750641
MSV3drs63750641
GWAS Ctlgrs63750641
Max Magnitude0
ClinVar
Risk rs63750641(G;G)
Alt rs63750641(G;G)
Reference rs63750641(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37042488A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075606.2,