rs1057517895

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1057517895(G;T)

Make rs1057517895(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

22

Position

49913603

Gene

ALG12

is a	snp
is	mentioned by
dbSNP	rs1057517895
dbSNP (classic)	rs1057517895
ClinGen	rs1057517895
ebi	rs1057517895
HLI	rs1057517895
Exac	rs1057517895
Gnomad	rs1057517895
Varsome	rs1057517895
LitVar	rs1057517895
Map	rs1057517895
PheGenI	rs1057517895
Biobank	rs1057517895
1000 genomes	rs1057517895
hgdp	rs1057517895
ensembl	rs1057517895
geneview	rs1057517895
scholar	rs1057517895
google	rs1057517895
pharmgkb	rs1057517895
gwascentral	rs1057517895
openSNP	rs1057517895
23andMe	rs1057517895
SNPshot	rs1057517895
SNPdbe	rs1057517895
MSV3d	rs1057517895
GWAS Ctlg	rs1057517895

Max Magnitude

0

ClinVar
Risk	rs1057517895(T;T)
Alt	rs1057517895(T;T)
Reference	Rs1057517895(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ALG12
CLNDBN	not provided
Reversed	1
HGVS	NC_000022.10:g.50307251C>A
CLNSRC
CLNACC	RCV000414118.1,