rs35383149

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	0.5	likely to be benign

Make rs35383149(G;G)

Reference

GRCh38 38.1/142

Chromosome

1

Position

63406361

Gene

ALG6

is a	snp
is	mentioned by
dbSNP	rs35383149
dbSNP (classic)	rs35383149
ClinGen	rs35383149
ebi	rs35383149
HLI	rs35383149
Exac	rs35383149
Gnomad	rs35383149
Varsome	rs35383149
LitVar	rs35383149
Map	rs35383149
PheGenI	rs35383149
Biobank	rs35383149
1000 genomes	rs35383149
hgdp	rs35383149
ensembl	rs35383149
geneview	rs35383149
scholar	rs35383149
google	rs35383149
pharmgkb	rs35383149
gwascentral	rs35383149
openSNP	rs35383149
23andMe	rs35383149
SNPshot	rs35383149
SNPdbe	rs35383149
MSV3d	rs35383149
GWAS Ctlg	rs35383149

GMAF

0.01791

Max Magnitude

0.5

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	RCV000023375.4, RCV000081558.10,