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rs63750071

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs63750071(-;-)
Make rs63750071(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025952
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750071
ebirs63750071
HLIrs63750071
Exacrs63750071
Varsomers63750071
Maprs63750071
PheGenIrs63750071
hapmaprs63750071
1000 genomesrs63750071
hgdprs63750071
ensemblrs63750071
gopubmedrs63750071
geneviewrs63750071
scholarrs63750071
googlers63750071
pharmgkbrs63750071
gwascentralrs63750071
openSNPrs63750071
23andMers63750071
23andMe allrs63750071
SNP Nexus

SNPshotrs63750071
SNPdbers63750071
MSV3drs63750071
GWAS Ctlgrs63750071
Max Magnitude0
ClinVar
Risk rs63750071(;)
Alt rs63750071(;)
Reference rs63750071(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067443delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075178.2,