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rs1057519069

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519069(C;G)
Make rs1057519069(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position32039178
GeneCYP21A2
is asnp
is mentioned by
dbSNPrs1057519069
dbSNP (old)rs1057519069
ClinGenrs1057519069
ebirs1057519069
HLIrs1057519069
Exacrs1057519069
Gnomadrs1057519069
Varsomers1057519069
Maprs1057519069
PheGenIrs1057519069
Biobankrs1057519069
1000 genomesrs1057519069
hgdprs1057519069
ensemblrs1057519069
gopubmedrs1057519069
geneviewrs1057519069
scholarrs1057519069
googlers1057519069
pharmgkbrs1057519069
gwascentralrs1057519069
openSNPrs1057519069
23andMers1057519069
23andMe allrs1057519069
SNPshotrs1057519069
SNPdbers1057519069
MSV3drs1057519069
GWAS Ctlgrs1057519069
Max Magnitude0
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,