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rs63750850

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750850(A;A)
Make rs63750850(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position36996689
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750850
ebirs63750850
HLIrs63750850
Exacrs63750850
Varsomers63750850
Maprs63750850
PheGenIrs63750850
hapmaprs63750850
1000 genomesrs63750850
hgdprs63750850
ensemblrs63750850
gopubmedrs63750850
geneviewrs63750850
scholarrs63750850
googlers63750850
pharmgkbrs63750850
gwascentralrs63750850
openSNPrs63750850
23andMers63750850
23andMe allrs63750850
SNP Nexus

SNPshotrs63750850
SNPdbers63750850
MSV3drs63750850
GWAS Ctlgrs63750850
Max Magnitude0
ClinVar
Risk rs63750850(A;A)
Alt rs63750850(A;A)
Reference rs63750850(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000003.11:g.37038180G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075399.2, RCV000160535.4, RCV000212515.1,