rs12032814

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	Likely to be a benign variant
(A;T)	0	Likely benign variant
(T;T)	0	common in clinvar

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

9247171

Gene

H6PD

is a	snp
is	mentioned by
dbSNP	rs12032814
dbSNP (classic)	rs12032814
ClinGen	rs12032814
ebi	rs12032814
HLI	rs12032814
Exac	rs12032814
Gnomad	rs12032814
Varsome	rs12032814
LitVar	rs12032814
Map	rs12032814
PheGenI	rs12032814
Biobank	rs12032814
1000 genomes	rs12032814
hgdp	rs12032814
ensembl	rs12032814
geneview	rs12032814
scholar	rs12032814
google	rs12032814
pharmgkb	rs12032814
gwascentral	rs12032814
openSNP	rs12032814
23andMe	rs12032814
SNPshot	rs12032814
SNPdbe	rs12032814
MSV3d	rs12032814
GWAS Ctlg	rs12032814

Max Magnitude

0

ClinVar
Risk	Rs12032814(A;A)
Alt	Rs12032814(A;A)
Reference	Rs12032814(T;T)
Significance	Probable-non-pathogenic
Disease	not specified
Variation	info
Gene	H6PD
CLNDBN	not specified
Reversed	0
HGVS	NC_000001.10:g.9307230T>A
CLNSRC
CLNACC	RCV000171451.2,