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rs587778955

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778955(A;A)
Make rs587778955(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36996691
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778955
ebirs587778955
HLIrs587778955
Exacrs587778955
Varsomers587778955
Maprs587778955
PheGenIrs587778955
hapmaprs587778955
1000 genomesrs587778955
hgdprs587778955
ensemblrs587778955
gopubmedrs587778955
geneviewrs587778955
scholarrs587778955
googlers587778955
pharmgkbrs587778955
gwascentralrs587778955
openSNPrs587778955
23andMers587778955
23andMe allrs587778955
SNP Nexus

SNPshotrs587778955
SNPdbers587778955
MSV3drs587778955
GWAS Ctlgrs587778955
Max Magnitude0
ClinVar
Risk rs587778955(A,T;A,T)
Alt rs587778955(A,T;A,T)
Reference rs587778955(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038182C>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075413.2,