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rs63750472

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750472(-;-)
Make rs63750472(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025659
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750472
ebirs63750472
HLIrs63750472
Exacrs63750472
Varsomers63750472
Maprs63750472
PheGenIrs63750472
hapmaprs63750472
1000 genomesrs63750472
hgdprs63750472
ensemblrs63750472
gopubmedrs63750472
geneviewrs63750472
scholarrs63750472
googlers63750472
pharmgkbrs63750472
gwascentralrs63750472
openSNPrs63750472
23andMers63750472
23andMe allrs63750472
SNP Nexus

SNPshotrs63750472
SNPdbers63750472
MSV3drs63750472
GWAS Ctlgrs63750472
Max Magnitude0
ClinVar
Risk rs63750472(;)
Alt rs63750472(;)
Reference rs63750472(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067150delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075105.2,