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rs587779976

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779976(C;T)
Make rs587779976(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47403261
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779976
ebirs587779976
HLIrs587779976
Exacrs587779976
Varsomers587779976
Maprs587779976
PheGenIrs587779976
hapmaprs587779976
1000 genomesrs587779976
hgdprs587779976
ensemblrs587779976
gopubmedrs587779976
geneviewrs587779976
scholarrs587779976
googlers587779976
pharmgkbrs587779976
gwascentralrs587779976
openSNPrs587779976
23andMers587779976
23andMe allrs587779976
SNP Nexus

SNPshotrs587779976
SNPdbers587779976
MSV3drs587779976
GWAS Ctlgrs587779976
Max Magnitude0
ClinVar
Risk rs587779976(T;T)
Alt rs587779976(T;T)
Reference rs587779976(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47630400C>T
CLNSRC
CLNACC RCV000115541.3,