Have questions? Visit https://www.reddit.com/r/SNPedia

rs765191836

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs765191836(G;T)
Make rs765191836(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position55367628
GeneSRD5A3, SRD5A3-AS1
is asnp
is mentioned by
dbSNPrs765191836
ebirs765191836
HLIrs765191836
Exacrs765191836
Varsomers765191836
Maprs765191836
PheGenIrs765191836
hapmaprs765191836
1000 genomesrs765191836
hgdprs765191836
ensemblrs765191836
gopubmedrs765191836
geneviewrs765191836
scholarrs765191836
googlers765191836
pharmgkbrs765191836
gwascentralrs765191836
openSNPrs765191836
23andMers765191836
23andMe allrs765191836
SNP Nexus

SNPshotrs765191836
SNPdbers765191836
MSV3drs765191836
GWAS Ctlgrs765191836
Max Magnitude0
ClinVar
Risk rs765191836(T;T)
Alt rs765191836(T;T)
Reference rs765191836(G;G)
Significance Pathogenic
Disease Congenital disorder of glycosylation type 1Q
Variation info
Gene SRD5A3 SRD5A3-AS1
CLNDBN Congenital disorder of glycosylation type 1Q
Reversed 0
HGVS NC_000004.11:g.56233795G>A
CLNSRC
CLNACC RCV000178363.1,