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rs63750561

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750561(A;A)
Make rs63750561(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37050517
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750561
ebirs63750561
HLIrs63750561
Exacrs63750561
Varsomers63750561
Maprs63750561
PheGenIrs63750561
hapmaprs63750561
1000 genomesrs63750561
hgdprs63750561
ensemblrs63750561
gopubmedrs63750561
geneviewrs63750561
scholarrs63750561
googlers63750561
pharmgkbrs63750561
gwascentralrs63750561
openSNPrs63750561
23andMers63750561
23andMe allrs63750561
SNP Nexus

SNPshotrs63750561
SNPdbers63750561
MSV3drs63750561
GWAS Ctlgrs63750561
Max Magnitude0
ClinVar
Risk rs63750561(A,T;A,T)
Alt rs63750561(A,T;A,T)
Reference rs63750561(G;G)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37092008G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075550.2, RCV000202047.1,