rs780420901

Orientation

plus

Stabilized

plus

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

Make rs780420901(G;T)

Make rs780420901(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

8073215

Gene

ALOX12B

is a	snp
is	mentioned by
dbSNP	rs780420901
dbSNP (classic)	rs780420901
ClinGen	rs780420901
ebi	rs780420901
HLI	rs780420901
Exac	rs780420901
Gnomad	rs780420901
Varsome	rs780420901
LitVar	rs780420901
Map	rs780420901
PheGenI	rs780420901
Biobank	rs780420901
1000 genomes	rs780420901
hgdp	rs780420901
ensembl	rs780420901
geneview	rs780420901
scholar	rs780420901
google	rs780420901
pharmgkb	rs780420901
gwascentral	rs780420901
openSNP	rs780420901
23andMe	rs780420901
SNPshot	rs780420901
SNPdbe	rs780420901
MSV3d	rs780420901
GWAS Ctlg	rs780420901

Max Magnitude

0

ClinVar
Risk	rs780420901(T;T)
Alt	rs780420901(T;T)
Reference	Rs780420901(G;G)
Significance	Pathogenic
Disease	Ichthyosis
Variation	info
Gene	ALOX12B
CLNDBN	Ichthyosis
Reversed	0
HGVS	NC_000017.10:g.7976533G>T
CLNSRC
CLNACC	RCV000414766.1,