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rs559947967

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs559947967(A;A)
Make rs559947967(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position33013356
GeneAK2
is asnp
is mentioned by
dbSNPrs559947967
ebirs559947967
HLIrs559947967
Exacrs559947967
Varsomers559947967
Maprs559947967
PheGenIrs559947967
hapmaprs559947967
1000 genomesrs559947967
hgdprs559947967
ensemblrs559947967
gopubmedrs559947967
geneviewrs559947967
scholarrs559947967
googlers559947967
pharmgkbrs559947967
gwascentralrs559947967
openSNPrs559947967
23andMers559947967
23andMe allrs559947967
SNP Nexus

SNPshotrs559947967
SNPdbers559947967
MSV3drs559947967
GWAS Ctlgrs559947967
Max Magnitude0
ClinVar
Risk rs559947967(A;A)
Alt rs559947967(A;A)
Reference rs559947967(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AK2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.33478957G>T
CLNSRC
CLNACC RCV000171151.1,