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rs267607093

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607093(A;A)
Make rs267607093(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position55359444
GeneSRD5A3
is asnp
is mentioned by
dbSNPrs267607093
ebirs267607093
HLIrs267607093
Exacrs267607093
Varsomers267607093
Maprs267607093
PheGenIrs267607093
hapmaprs267607093
1000 genomesrs267607093
hgdprs267607093
ensemblrs267607093
gopubmedrs267607093
geneviewrs267607093
scholarrs267607093
googlers267607093
pharmgkbrs267607093
gwascentralrs267607093
openSNPrs267607093
23andMers267607093
23andMe allrs267607093
SNP Nexus

SNPshotrs267607093
SNPdbers267607093
MSV3drs267607093
GWAS Ctlgrs267607093
Max Magnitude0
ClinVar
Risk rs267607093(A;A)
Alt rs267607093(A;A)
Reference rs267607093(G;G)
Significance Pathogenic
Disease Congenital disorder of glycosylation type 1Q
Variation info
Gene SRD5A3
CLNDBN Congenital disorder of glycosylation type 1Q
Reversed 0
HGVS NC_000004.11:g.56225611G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000891.2,