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rs35383149

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 0.5 likely to be benign
Make rs35383149(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position63406361
GeneALG6
is asnp
is mentioned by
dbSNPrs35383149
ebirs35383149
HLIrs35383149
Exacrs35383149
Varsomers35383149
Maprs35383149
PheGenIrs35383149
hapmaprs35383149
1000 genomesrs35383149
hgdprs35383149
ensemblrs35383149
gopubmedrs35383149
geneviewrs35383149
scholarrs35383149
googlers35383149
pharmgkbrs35383149
gwascentralrs35383149
openSNPrs35383149
23andMers35383149
23andMe allrs35383149
SNP Nexus

SNPshotrs35383149
SNPdbers35383149
MSV3drs35383149
GWAS Ctlgrs35383149
GMAF0.01791
Max Magnitude0.5
ClinVar
Risk rs35383149(G;G)
Alt rs35383149(G;G)
Reference rs35383149(A;A)
Significance Other
Disease Congenital disorder of glycosylation type 1C not specified
Variation info
Gene ALG6
CLNDBN Congenital disorder of glycosylation type 1C not specified
Reversed 1
HGVS NC_000001.10:g.63872032T>C
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000023375.3, RCV000081558.8,