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rs63750549

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750549(A;A)
Make rs63750549(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37048532
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750549
ebirs63750549
HLIrs63750549
Exacrs63750549
Varsomers63750549
Maprs63750549
PheGenIrs63750549
hapmaprs63750549
1000 genomesrs63750549
hgdprs63750549
ensemblrs63750549
gopubmedrs63750549
geneviewrs63750549
scholarrs63750549
googlers63750549
pharmgkbrs63750549
gwascentralrs63750549
openSNPrs63750549
23andMers63750549
23andMe allrs63750549
SNP Nexus

SNPshotrs63750549
SNPdbers63750549
MSV3drs63750549
GWAS Ctlgrs63750549
Max Magnitude0
ClinVar
Risk rs63750549(A,T;A,T)
Alt rs63750549(A,T;A,T)
Reference rs63750549(G;G)
Significance Pathogenic
Disease not provided Lynch syndrome
Variation info
Gene MLH1
CLNDBN not provided Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090023G>A; NC_000003.11:g.37090023G>T
CLNSRC
CLNACC RCV000114854.1, RCV000197271.1,