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rs79716074

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs79716074(A;G)
Make rs79716074(G;G)
ReferenceGRCh37.p5 37.3/135
Chromosome2
Position277003
GeneACP1
is asnp
is mentioned by
dbSNPrs79716074
ebirs79716074
HLIrs79716074
Exacrs79716074
Varsomers79716074
Maprs79716074
PheGenIrs79716074
hapmaprs79716074
1000 genomesrs79716074
hgdprs79716074
ensemblrs79716074
gopubmedrs79716074
geneviewrs79716074
scholarrs79716074
googlers79716074
pharmgkbrs79716074
gwascentralrs79716074
openSNPrs79716074
23andMers79716074
23andMe allrs79716074
SNP Nexus

SNPshotrs79716074
SNPdbers79716074
MSV3drs79716074
GWAS Ctlgrs79716074
Merged fromRs7576247
GMAF0.2525
Max Magnitude0
OMIM171500
Desc
Variant0001
Relatedalso
ClinVar
Risk rs79716074(G;G)
Alt rs79716074(G;G)
Reference rs79716074(A;A)
Significance Non-pathogenic
Disease ACID PHOSPHATASE 1
Variation info
Gene ACP1
CLNDBN ACID PHOSPHATASE 1, SOLUBLE, A/B POLYMORPHISM OF
Reversed 0
HGVS NC_000002.11:g.277003A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014681.2,