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rs757156390

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757156390(A;A)
Make rs757156390(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position123332657
GeneADCY5
is asnp
is mentioned by
dbSNPrs757156390
ebirs757156390
HLIrs757156390
Exacrs757156390
Varsomers757156390
Maprs757156390
PheGenIrs757156390
hapmaprs757156390
1000 genomesrs757156390
hgdprs757156390
ensemblrs757156390
gopubmedrs757156390
geneviewrs757156390
scholarrs757156390
googlers757156390
pharmgkbrs757156390
gwascentralrs757156390
openSNPrs757156390
23andMers757156390
23andMe allrs757156390
SNP Nexus

SNPshotrs757156390
SNPdbers757156390
MSV3drs757156390
GWAS Ctlgrs757156390
Max Magnitude0
ClinVar
Risk rs757156390(A;A)
Alt rs757156390(A;A)
Reference rs757156390(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ADCY5
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000003.11:g.123051504G>C
CLNSRC
CLNACC RCV000190681.1,