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rs748318386

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs748318386(A;A)
Make rs748318386(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position91220824
GeneAUH
is asnp
is mentioned by
dbSNPrs748318386
ebirs748318386
HLIrs748318386
Exacrs748318386
Varsomers748318386
Maprs748318386
PheGenIrs748318386
hapmaprs748318386
1000 genomesrs748318386
hgdprs748318386
ensemblrs748318386
gopubmedrs748318386
geneviewrs748318386
scholarrs748318386
googlers748318386
pharmgkbrs748318386
gwascentralrs748318386
openSNPrs748318386
23andMers748318386
23andMe allrs748318386
SNP Nexus

SNPshotrs748318386
SNPdbers748318386
MSV3drs748318386
GWAS Ctlgrs748318386
Max Magnitude0
ClinVar
Risk rs748318386(A;A)
Alt rs748318386(A;A)
Reference rs748318386(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AUH
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.93983106G>A
CLNSRC
CLNACC RCV000196487.1,