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rs794729223

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs794729223(-;-)
Make rs794729223(-;AG)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153798075
GeneSSR4
is asnp
is mentioned by
dbSNPrs794729223
dbSNP (old)rs794729223
ClinGenrs794729223
ebirs794729223
HLIrs794729223
Exacrs794729223
Gnomadrs794729223
Varsomers794729223
Maprs794729223
PheGenIrs794729223
Biobankrs794729223
1000 genomesrs794729223
hgdprs794729223
ensemblrs794729223
gopubmedrs794729223
geneviewrs794729223
scholarrs794729223
googlers794729223
pharmgkbrs794729223
gwascentralrs794729223
openSNPrs794729223
23andMers794729223
23andMe allrs794729223
SNP Nexus

SNPshotrs794729223
SNPdbers794729223
MSV3drs794729223
GWAS Ctlgrs794729223
Max Magnitude0
ClinVar
Risk rs794729223(-;-)
Alt rs794729223(-;-)
Reference Rs794729223(AG;AG)
Significance Other
Disease Congenital disorder of glycosylation type 1y
Variation info
Gene SSR4
CLNDBN Congenital disorder of glycosylation type 1y
Reversed 0
HGVS NC_000023.10:g.153063532_153063533delAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000412666.2,