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rs587779941

From SNPedia

Orientationplus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs587779941(-;-)
Make rs587779941(-;AAAG)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47795904
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779941
ebirs587779941
HLIrs587779941
Exacrs587779941
Varsomers587779941
Maprs587779941
PheGenIrs587779941
hapmaprs587779941
1000 genomesrs587779941
hgdprs587779941
ensemblrs587779941
gopubmedrs587779941
geneviewrs587779941
scholarrs587779941
googlers587779941
pharmgkbrs587779941
gwascentralrs587779941
openSNPrs587779941
23andMers587779941
23andMe allrs587779941
SNP Nexus

SNPshotrs587779941
SNPdbers587779941
MSV3drs587779941
GWAS Ctlgrs587779941
Max Magnitude0
ClinVar
Risk rs587779941(;)
Alt rs587779941(;)
Reference rs587779941(AAAG;AAAG)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48023043_48023046delAAAG
CLNSRC
CLNACC RCV000115431.3,