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rs886038207

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs886038207(-;-)
Make rs886038207(-;CT)
ReferenceGRCh38.p7 38.3/149
Chromosome6
Position32038580
GeneCYP21A2
is asnp
is mentioned by
dbSNPrs886038207
dbSNP (classic)rs886038207
ClinGenrs886038207
ebirs886038207
HLIrs886038207
Exacrs886038207
Gnomadrs886038207
Varsomers886038207
LitVarrs886038207
Maprs886038207
PheGenIrs886038207
Biobankrs886038207
1000 genomesrs886038207
hgdprs886038207
ensemblrs886038207
geneviewrs886038207
scholarrs886038207
googlers886038207
pharmgkbrs886038207
gwascentralrs886038207
openSNPrs886038207
23andMers886038207
23andMe allrs886038207
SNPshotrs886038207
SNPdbers886038207
MSV3drs886038207
GWAS Ctlgrs886038207
Max Magnitude0
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,