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rs587778900

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587778900(-;-)
Make rs587778900(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37025816
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778900
ebirs587778900
HLIrs587778900
Exacrs587778900
Varsomers587778900
Maprs587778900
PheGenIrs587778900
hapmaprs587778900
1000 genomesrs587778900
hgdprs587778900
ensemblrs587778900
gopubmedrs587778900
geneviewrs587778900
scholarrs587778900
googlers587778900
pharmgkbrs587778900
gwascentralrs587778900
openSNPrs587778900
23andMers587778900
23andMe allrs587778900
SNP Nexus

SNPshotrs587778900
SNPdbers587778900
MSV3drs587778900
GWAS Ctlgrs587778900
Max Magnitude0
ClinVar
Risk rs587778900(;)
Alt rs587778900(;)
Reference rs587778900(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067307delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075154.2,