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rs587779914

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779914(A;A)
Make rs587779914(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799224
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779914
ebirs587779914
HLIrs587779914
Exacrs587779914
Varsomers587779914
Maprs587779914
PheGenIrs587779914
hapmaprs587779914
1000 genomesrs587779914
hgdprs587779914
ensemblrs587779914
gopubmedrs587779914
geneviewrs587779914
scholarrs587779914
googlers587779914
pharmgkbrs587779914
gwascentralrs587779914
openSNPrs587779914
23andMers587779914
23andMe allrs587779914
SNP Nexus

SNPshotrs587779914
SNPdbers587779914
MSV3drs587779914
GWAS Ctlgrs587779914
Max Magnitude0
ClinVar
Risk rs587779914(A;A)
Alt rs587779914(A;A)
Reference rs587779914(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48026363G>A
CLNSRC
CLNACC RCV000115372.2,