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rs63750500

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750500(A;T)
Make rs63750500(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37011860
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750500
ebirs63750500
HLIrs63750500
Exacrs63750500
Varsomers63750500
Maprs63750500
PheGenIrs63750500
hapmaprs63750500
1000 genomesrs63750500
hgdprs63750500
ensemblrs63750500
gopubmedrs63750500
geneviewrs63750500
scholarrs63750500
googlers63750500
pharmgkbrs63750500
gwascentralrs63750500
openSNPrs63750500
23andMers63750500
23andMe allrs63750500
SNP Nexus

SNPshotrs63750500
SNPdbers63750500
MSV3drs63750500
GWAS Ctlgrs63750500
Max Magnitude0
ClinVar
Risk rs63750500(T;T)
Alt rs63750500(T;T)
Reference rs63750500(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053351A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075768.2,