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rs730880982

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880982(A;C)
Make rs730880982(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position151560556
GenePRKAG2
is asnp
is mentioned by
dbSNPrs730880982
ebirs730880982
HLIrs730880982
Exacrs730880982
Varsomers730880982
Maprs730880982
PheGenIrs730880982
hapmaprs730880982
1000 genomesrs730880982
hgdprs730880982
ensemblrs730880982
gopubmedrs730880982
geneviewrs730880982
scholarrs730880982
googlers730880982
pharmgkbrs730880982
gwascentralrs730880982
openSNPrs730880982
23andMers730880982
23andMe allrs730880982
SNP Nexus

SNPshotrs730880982
SNPdbers730880982
MSV3drs730880982
GWAS Ctlgrs730880982
Max Magnitude0
ClinVar
Risk rs730880982(C;C)
Alt rs730880982(C;C)
Reference rs730880982(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PRKAG2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.151257642T>G
CLNSRC
CLNACC RCV000159021.2,