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rs587778907

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778907(-;-)
Make rs587778907(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37025960
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778907
ebirs587778907
HLIrs587778907
Exacrs587778907
Varsomers587778907
Maprs587778907
PheGenIrs587778907
hapmaprs587778907
1000 genomesrs587778907
hgdprs587778907
ensemblrs587778907
gopubmedrs587778907
geneviewrs587778907
scholarrs587778907
googlers587778907
pharmgkbrs587778907
gwascentralrs587778907
openSNPrs587778907
23andMers587778907
23andMe allrs587778907
SNP Nexus

SNPshotrs587778907
SNPdbers587778907
MSV3drs587778907
GWAS Ctlgrs587778907
Max Magnitude0
ClinVar
Risk rs587778907(;)
Alt rs587778907(;)
Reference rs587778907(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067451delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075180.2,