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rs63750035

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(I;I) 0
Make rs63750035(-;-)
Make rs63750035(-;AG)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047570
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750035
ebirs63750035
HLIrs63750035
Exacrs63750035
Varsomers63750035
Maprs63750035
PheGenIrs63750035
hapmaprs63750035
1000 genomesrs63750035
hgdprs63750035
ensemblrs63750035
gopubmedrs63750035
geneviewrs63750035
scholarrs63750035
googlers63750035
pharmgkbrs63750035
gwascentralrs63750035
openSNPrs63750035
23andMers63750035
23andMe allrs63750035
SNP Nexus

SNPshotrs63750035
SNPdbers63750035
MSV3drs63750035
GWAS Ctlgrs63750035
Max Magnitude0
ClinVar
Risk rs63750035(;)
Alt rs63750035(;)
Reference rs63750035(AG;AG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089061_37089062delAG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075364.2,