rs886039748

Orientation

minus

Stabilized

minus

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

Make rs886039748(C;C)

Make rs886039748(C;T)

Reference

GRCh38.p7 38.3/149

Chromosome

2

Position

31580899

Gene

SRD5A2

is a	snp
is	mentioned by
dbSNP	rs886039748
dbSNP (classic)	rs886039748
ClinGen	rs886039748
ebi	rs886039748
HLI	rs886039748
Exac	rs886039748
Gnomad	rs886039748
Varsome	rs886039748
LitVar	rs886039748
Map	rs886039748
PheGenI	rs886039748
Biobank	rs886039748
1000 genomes	rs886039748
hgdp	rs886039748
ensembl	rs886039748
geneview	rs886039748
scholar	rs886039748
google	rs886039748
pharmgkb	rs886039748
gwascentral	rs886039748
openSNP	rs886039748
23andMe	rs886039748
SNPshot	rs886039748
SNPdbe	rs886039748
MSV3d	rs886039748
GWAS Ctlg	rs886039748

Max Magnitude

0

ClinVar
Risk	rs886039748(C;C)
Alt	rs886039748(C;C)
Reference	Rs886039748(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SRD5A2
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.31805968A>G
CLNSRC
CLNACC	RCV000254818.1,