Rs104894150

From SNPedia
Jump to: navigation, search

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894150(A;A)
Make rs104894150(A;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position102834850
GeneCYP17A1, CYP17A1-AS1
is asnp
is mentioned by
dbSNPrs104894150
Exacrs104894150
PheGenIrs104894150
nextbiors104894150
hapmaprs104894150
1000 genomesrs104894150
hgdprs104894150
ensemblrs104894150
gopubmedrs104894150
geneviewrs104894150
scholarrs104894150
googlers104894150
pharmgkbrs104894150
gwascentralrs104894150
openSNPrs104894150
23andMers104894150
23andMe allrs104894150
SNP Nexus

SNPshotrs104894150
SNPdbers104894150
MSV3drs104894150
Max Magnitude0
OMIM609300
Desc
Variant0027
Relatedalso
ClinVar
Risk rs104894150(A;A)
Alt rs104894150(A;A)
Reference rs104894150(T;T)
Significance Pathogenic
Disease Combined partial 17-alpha-hydroxylase/17
Variation info
Gene CYP17A1
CLNDBN Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency
Reversed 1
HGVS NC_000010.10:g.104594607A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001873.1,