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rs587781544

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781544(-;-)
Make rs587781544(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47803663
GeneMSH6
is asnp
is mentioned by
dbSNPrs587781544
ebirs587781544
HLIrs587781544
Exacrs587781544
Varsomers587781544
Maprs587781544
PheGenIrs587781544
hapmaprs587781544
1000 genomesrs587781544
hgdprs587781544
ensemblrs587781544
gopubmedrs587781544
geneviewrs587781544
scholarrs587781544
googlers587781544
pharmgkbrs587781544
gwascentralrs587781544
openSNPrs587781544
23andMers587781544
23andMe allrs587781544
SNP Nexus

SNPshotrs587781544
SNPdbers587781544
MSV3drs587781544
GWAS Ctlgrs587781544
Max Magnitude0
ClinVar
Risk rs587781544(;)
Alt rs587781544(;)
Reference rs587781544(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.48030802delG
CLNSRC
CLNACC RCV000129558.2,