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rs587778962

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778962(-;-)
Make rs587778962(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37048550
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778962
ebirs587778962
HLIrs587778962
Exacrs587778962
Varsomers587778962
Maprs587778962
PheGenIrs587778962
hapmaprs587778962
1000 genomesrs587778962
hgdprs587778962
ensemblrs587778962
gopubmedrs587778962
geneviewrs587778962
scholarrs587778962
googlers587778962
pharmgkbrs587778962
gwascentralrs587778962
openSNPrs587778962
23andMers587778962
23andMe allrs587778962
SNP Nexus

SNPshotrs587778962
SNPdbers587778962
MSV3drs587778962
GWAS Ctlgrs587778962
Max Magnitude0
ClinVar
Risk rs587778962(;)
Alt rs587778962(;)
Reference rs587778962(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090041delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075429.2,