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rs63750434

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750434(-;-)
Make rs63750434(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020432
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750434
ebirs63750434
HLIrs63750434
Exacrs63750434
Varsomers63750434
Maprs63750434
PheGenIrs63750434
hapmaprs63750434
1000 genomesrs63750434
hgdprs63750434
ensemblrs63750434
gopubmedrs63750434
geneviewrs63750434
scholarrs63750434
googlers63750434
pharmgkbrs63750434
gwascentralrs63750434
openSNPrs63750434
23andMers63750434
23andMe allrs63750434
SNP Nexus

SNPshotrs63750434
SNPdbers63750434
MSV3drs63750434
GWAS Ctlgrs63750434
Max Magnitude0
ClinVar
Risk rs63750434(;)
Alt rs63750434(;)
Reference rs63750434(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061923delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075071.2,