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rs63750645

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(I;I) 0
Make rs63750645(-;-)
Make rs63750645(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37004435
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750645
ebirs63750645
HLIrs63750645
Exacrs63750645
Varsomers63750645
Maprs63750645
PheGenIrs63750645
hapmaprs63750645
1000 genomesrs63750645
hgdprs63750645
ensemblrs63750645
gopubmedrs63750645
geneviewrs63750645
scholarrs63750645
googlers63750645
pharmgkbrs63750645
gwascentralrs63750645
openSNPrs63750645
23andMers63750645
23andMe allrs63750645
SNP Nexus

SNPshotrs63750645
SNPdbers63750645
MSV3drs63750645
GWAS Ctlgrs63750645
Max Magnitude0
ClinVar
Risk rs63750645(;)
Alt rs63750645(;)
Reference rs63750645(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37045926delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075660.2,