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rs63750962

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63750962(-;-)
Make rs63750962(-;GC)
Make rs63750962(GC;GC)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020347
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750962
ebirs63750962
HLIrs63750962
Exacrs63750962
Varsomers63750962
Maprs63750962
PheGenIrs63750962
hapmaprs63750962
1000 genomesrs63750962
hgdprs63750962
ensemblrs63750962
gopubmedrs63750962
geneviewrs63750962
scholarrs63750962
googlers63750962
pharmgkbrs63750962
gwascentralrs63750962
openSNPrs63750962
23andMers63750962
23andMe allrs63750962
SNP Nexus

SNPshotrs63750962
SNPdbers63750962
MSV3drs63750962
GWAS Ctlgrs63750962
Max Magnitude0
ClinVar
Risk rs63750962(GC;GC)
Alt rs63750962(GC;GC)
Reference rs63750962(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061837_37061838dupGC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075936.2,