Have questions? Visit https://www.reddit.com/r/SNPedia

rs61752479

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61752479(A;A)
Make rs61752479(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position114688633
GeneAMPD1
is asnp
is mentioned by
dbSNPrs61752479
ebirs61752479
HLIrs61752479
Exacrs61752479
Varsomers61752479
Maprs61752479
PheGenIrs61752479
hapmaprs61752479
1000 genomesrs61752479
hgdprs61752479
ensemblrs61752479
gopubmedrs61752479
geneviewrs61752479
scholarrs61752479
googlers61752479
pharmgkbrs61752479
gwascentralrs61752479
openSNPrs61752479
23andMers61752479
23andMe allrs61752479
SNP Nexus

SNPshotrs61752479
SNPdbers61752479
MSV3drs61752479
GWAS Ctlgrs61752479
Max Magnitude0
ClinVar
Risk rs61752479(A;A)
Alt rs61752479(A;A)
Reference rs61752479(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene AMPD1
CLNDBN not provided
Reversed 0
HGVS NC_000001.11:g.114688633G>A
CLNSRC ClinVar Emory University GTR
CLNACC RCV000077975.1,