rs748318386

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs748318386(A;A)

Make rs748318386(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

91220824

Gene

AUH

is a	snp
is	mentioned by
dbSNP	rs748318386
dbSNP (classic)	rs748318386
ClinGen	rs748318386
ebi	rs748318386
HLI	rs748318386
Exac	rs748318386
Gnomad	rs748318386
Varsome	rs748318386
LitVar	rs748318386
Map	rs748318386
PheGenI	rs748318386
Biobank	rs748318386
1000 genomes	rs748318386
hgdp	rs748318386
ensembl	rs748318386
geneview	rs748318386
scholar	rs748318386
google	rs748318386
pharmgkb	rs748318386
gwascentral	rs748318386
openSNP	rs748318386
23andMe	rs748318386
SNPshot	rs748318386
SNPdbe	rs748318386
MSV3d	rs748318386
GWAS Ctlg	rs748318386

Max Magnitude

0

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,