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rs554853074

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs554853074(C;C)
Make rs554853074(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position44160215
GeneJPH2
is asnp
is mentioned by
dbSNPrs554853074
ebirs554853074
HLIrs554853074
Exacrs554853074
Varsomers554853074
Maprs554853074
PheGenIrs554853074
hapmaprs554853074
1000 genomesrs554853074
hgdprs554853074
ensemblrs554853074
gopubmedrs554853074
geneviewrs554853074
scholarrs554853074
googlers554853074
pharmgkbrs554853074
gwascentralrs554853074
openSNPrs554853074
23andMers554853074
23andMe allrs554853074
SNP Nexus

SNPshotrs554853074
SNPdbers554853074
MSV3drs554853074
GWAS Ctlgrs554853074
Max Magnitude0
ClinVar
Risk rs554853074(C;C)
Alt rs554853074(C;C)
Reference rs554853074(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene JPH2
CLNDBN not specified
Reversed 0
HGVS NC_000020.10:g.42788855G>C
CLNSRC
CLNACC RCV000223019.2,