rs1057519069

Orientation

plus

Stabilized

plus

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

Make rs1057519069(C;G)

Make rs1057519069(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

32039178

Gene

CYP21A2

is a	snp
is	mentioned by
dbSNP	rs1057519069
dbSNP (classic)	rs1057519069
ClinGen	rs1057519069
ebi	rs1057519069
HLI	rs1057519069
Exac	rs1057519069
Gnomad	rs1057519069
Varsome	rs1057519069
LitVar	rs1057519069
Map	rs1057519069
PheGenI	rs1057519069
Biobank	rs1057519069
1000 genomes	rs1057519069
hgdp	rs1057519069
ensembl	rs1057519069
geneview	rs1057519069
scholar	rs1057519069
google	rs1057519069
pharmgkb	rs1057519069
gwascentral	rs1057519069
openSNP	rs1057519069
23andMe	rs1057519069
SNPshot	rs1057519069
SNPdbe	rs1057519069
MSV3d	rs1057519069
GWAS Ctlg	rs1057519069

Max Magnitude

0

ClinVar
Risk	rs1057519069(G;G)
Alt	rs1057519069(G;G)
Reference	Rs1057519069(C;C)
Significance	Pathogenic
Disease	21-hydroxylase deficiency
Variation	info
Gene	CYP21A2
CLNDBN	21-hydroxylase deficiency
Reversed	0
HGVS	NC_000006.11:g.32006955C>G
CLNSRC
CLNACC	RCV000416360.1,