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rs587779950

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779950(A;A)
Make rs587779950(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36996618
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779950
ebirs587779950
HLIrs587779950
Exacrs587779950
Varsomers587779950
Maprs587779950
PheGenIrs587779950
hapmaprs587779950
1000 genomesrs587779950
hgdprs587779950
ensemblrs587779950
gopubmedrs587779950
geneviewrs587779950
scholarrs587779950
googlers587779950
pharmgkbrs587779950
gwascentralrs587779950
openSNPrs587779950
23andMers587779950
23andMe allrs587779950
SNP Nexus

SNPshotrs587779950
SNPdbers587779950
MSV3drs587779950
GWAS Ctlgrs587779950
Max Magnitude0
ClinVar
Risk rs587779950(A;A)
Alt rs587779950(A;A)
Reference rs587779950(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37038109G>A
CLNSRC
CLNACC RCV000115453.2,