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rs587778908

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778908(-;-)
Make rs587778908(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37025975
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778908
ebirs587778908
HLIrs587778908
Exacrs587778908
Varsomers587778908
Maprs587778908
PheGenIrs587778908
hapmaprs587778908
1000 genomesrs587778908
hgdprs587778908
ensemblrs587778908
gopubmedrs587778908
geneviewrs587778908
scholarrs587778908
googlers587778908
pharmgkbrs587778908
gwascentralrs587778908
openSNPrs587778908
23andMers587778908
23andMe allrs587778908
SNP Nexus

SNPshotrs587778908
SNPdbers587778908
MSV3drs587778908
GWAS Ctlgrs587778908
Max Magnitude0
ClinVar
Risk rs587778908(;)
Alt rs587778908(;)
Reference rs587778908(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067466delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075182.2,