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rs148157596

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs148157596(A;A)
Make rs148157596(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position91220972
GeneAUH
is asnp
is mentioned by
dbSNPrs148157596
ebirs148157596
HLIrs148157596
Exacrs148157596
Varsomers148157596
Maprs148157596
PheGenIrs148157596
hapmaprs148157596
1000 genomesrs148157596
hgdprs148157596
ensemblrs148157596
gopubmedrs148157596
geneviewrs148157596
scholarrs148157596
googlers148157596
pharmgkbrs148157596
gwascentralrs148157596
openSNPrs148157596
23andMers148157596
23andMe allrs148157596
SNP Nexus

SNPshotrs148157596
SNPdbers148157596
MSV3drs148157596
GWAS Ctlgrs148157596
Max Magnitude0
ClinVar
Risk rs148157596(A;A)
Alt rs148157596(A;A)
Reference rs148157596(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene AUH
CLNDBN not specified
Reversed 0
HGVS NC_000009.11:g.93983254G>A
CLNSRC
CLNACC RCV000199924.2,