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rs587778927

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778927(-;-)
Make rs587778927(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36996658
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778927
ebirs587778927
HLIrs587778927
Exacrs587778927
Varsomers587778927
Maprs587778927
PheGenIrs587778927
hapmaprs587778927
1000 genomesrs587778927
hgdprs587778927
ensemblrs587778927
gopubmedrs587778927
geneviewrs587778927
scholarrs587778927
googlers587778927
pharmgkbrs587778927
gwascentralrs587778927
openSNPrs587778927
23andMers587778927
23andMe allrs587778927
SNP Nexus

SNPshotrs587778927
SNPdbers587778927
MSV3drs587778927
GWAS Ctlgrs587778927
Max Magnitude0
ClinVar
Risk rs587778927(;)
Alt rs587778927(;)
Reference rs587778927(A;A)
Significance Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37038149delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075267.2, RCV000213962.1,