Have questions? Visit https://www.reddit.com/r/SNPedia

rs63750547

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750547(G;G)
Make rs63750547(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020312
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750547
ebirs63750547
HLIrs63750547
Exacrs63750547
Varsomers63750547
Maprs63750547
PheGenIrs63750547
hapmaprs63750547
1000 genomesrs63750547
hgdprs63750547
ensemblrs63750547
gopubmedrs63750547
geneviewrs63750547
scholarrs63750547
googlers63750547
pharmgkbrs63750547
gwascentralrs63750547
openSNPrs63750547
23andMers63750547
23andMe allrs63750547
SNP Nexus

SNPshotrs63750547
SNPdbers63750547
MSV3drs63750547
GWAS Ctlgrs63750547
Max Magnitude0
ClinVar
Risk rs63750547(C,G;C,G)
Alt rs63750547(C,G;C,G)
Reference rs63750547(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Lynch syndrome
Variation info
Gene MLH1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061803T>C; NC_000003.11:g.37061803T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000222772.1, RCV000075923.2,