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rs730880981

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880981(C;C)
Make rs730880981(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position151564191
GenePRKAG2
is asnp
is mentioned by
dbSNPrs730880981
ebirs730880981
HLIrs730880981
Exacrs730880981
Varsomers730880981
Maprs730880981
PheGenIrs730880981
hapmaprs730880981
1000 genomesrs730880981
hgdprs730880981
ensemblrs730880981
gopubmedrs730880981
geneviewrs730880981
scholarrs730880981
googlers730880981
pharmgkbrs730880981
gwascentralrs730880981
openSNPrs730880981
23andMers730880981
23andMe allrs730880981
SNP Nexus

SNPshotrs730880981
SNPdbers730880981
MSV3drs730880981
GWAS Ctlgrs730880981
Max Magnitude0
ClinVar
Risk rs730880981(C;C)
Alt rs730880981(C;C)
Reference Rs730880981(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PRKAG2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.151261277C>G
CLNSRC
CLNACC RCV000159016.1,