rs1057518381

Orientation

minus

Stabilized

minus

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

Make rs1057518381(A;A)

Make rs1057518381(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

8080778

Gene	ALOX12B, LOC107985075

is a	snp
is	mentioned by
dbSNP	rs1057518381
dbSNP (classic)	rs1057518381
ClinGen	rs1057518381
ebi	rs1057518381
HLI	rs1057518381
Exac	rs1057518381
Gnomad	rs1057518381
Varsome	rs1057518381
LitVar	rs1057518381
Map	rs1057518381
PheGenI	rs1057518381
Biobank	rs1057518381
1000 genomes	rs1057518381
hgdp	rs1057518381
ensembl	rs1057518381
geneview	rs1057518381
scholar	rs1057518381
google	rs1057518381
pharmgkb	rs1057518381
gwascentral	rs1057518381
openSNP	rs1057518381
23andMe	rs1057518381
SNPshot	rs1057518381
SNPdbe	rs1057518381
MSV3d	rs1057518381
GWAS Ctlg	rs1057518381

Max Magnitude

0

ClinVar
Risk	rs1057518381(A;A)
Alt	rs1057518381(A;A)
Reference	Rs1057518381(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ALOX12B
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.7984096C>T
CLNSRC
CLNACC	RCV000413742.1,