rs886038207

Orientation

plus

Stabilized

plus

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

Make rs886038207(-;-)

Make rs886038207(-;CT)

Reference

GRCh38.p7 38.3/149

Chromosome

6

Position

32038580

Gene

CYP21A2

is a	snp
is	mentioned by
dbSNP	rs886038207
dbSNP (classic)	rs886038207
ClinGen	rs886038207
ebi	rs886038207
HLI	rs886038207
Exac	rs886038207
Gnomad	rs886038207
Varsome	rs886038207
LitVar	rs886038207
Map	rs886038207
PheGenI	rs886038207
Biobank	rs886038207
1000 genomes	rs886038207
hgdp	rs886038207
ensembl	rs886038207
geneview	rs886038207
scholar	rs886038207
google	rs886038207
pharmgkb	rs886038207
gwascentral	rs886038207
openSNP	rs886038207
23andMe	rs886038207
SNPshot	rs886038207
SNPdbe	rs886038207
MSV3d	rs886038207
GWAS Ctlg	rs886038207

Max Magnitude

0

ClinVar
Risk	rs886038207(-;-)
Alt	rs886038207(-;-)
Reference	Rs886038207(CT;CT)
Significance	Probable-Pathogenic
Disease	21-hydroxylase deficiency
Variation	info
Gene	CYP21A2
CLNDBN	21-hydroxylase deficiency
Reversed	0
HGVS	NC_000006.11:g.32006357_32006358delCT
CLNSRC
CLNACC	RCV000256427.1,