rs17855765

Orientation

plus

Stabilized

plus

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

Make rs17855765(C;T)

Make rs17855765(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

144415944

Gene

SLC39A4

is a	snp
is	mentioned by
dbSNP	rs17855765
dbSNP (classic)	rs17855765
ClinGen	rs17855765
ebi	rs17855765
HLI	rs17855765
Exac	rs17855765
Gnomad	rs17855765
Varsome	rs17855765
LitVar	rs17855765
Map	rs17855765
PheGenI	rs17855765
Biobank	rs17855765
1000 genomes	rs17855765
hgdp	rs17855765
ensembl	rs17855765
geneview	rs17855765
scholar	rs17855765
google	rs17855765
pharmgkb	rs17855765
gwascentral	rs17855765
openSNP	rs17855765
23andMe	rs17855765
SNPshot	rs17855765
SNPdbe	rs17855765
MSV3d	rs17855765
GWAS Ctlg	rs17855765

GMAF

0.4348

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

ClinVar
Risk	rs17855765(T;T)
Alt	rs17855765(T;T)
Reference	Rs17855765(C;C)
Significance	Non-pathogenic
Disease	Hereditary acrodermatitis enteropathica not specified
Variation	info
Gene	SLC39A4
CLNDBN	Hereditary acrodermatitis enteropathica not specified
Reversed	0
HGVS	NC_000008.10:g.145641328C>T
CLNSRC
CLNACC	RCV000359976.1, RCV000455765.1,