rs119471022

Orientation

minus

Stabilized

minus

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

Make rs119471022(C;T)

Make rs119471022(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

26470774

Gene

HPS4

is a	snp
is	mentioned by
dbSNP	rs119471022
dbSNP (classic)	rs119471022
ClinGen	rs119471022
ebi	rs119471022
HLI	rs119471022
Exac	rs119471022
Gnomad	rs119471022
Varsome	rs119471022
LitVar	rs119471022
Map	rs119471022
PheGenI	rs119471022
Biobank	rs119471022
1000 genomes	rs119471022
hgdp	rs119471022
ensembl	rs119471022
geneview	rs119471022
scholar	rs119471022
google	rs119471022
pharmgkb	rs119471022
gwascentral	rs119471022
openSNP	rs119471022
23andMe	rs119471022
SNPshot	rs119471022
SNPdbe	rs119471022
MSV3d	rs119471022
GWAS Ctlg	rs119471022

Max Magnitude

0

OMIM	606682
Desc
Variant	0004
Related	also

ClinVar
Risk	rs119471022(A;A) rs119471022(T;T)
Alt	rs119471022(A;A) rs119471022(T;T)
Reference	Rs119471022(C;C)
Significance	Pathogenic
Disease	Hermansky-Pudlak syndrome 4
Variation	info
Gene	HPS4
CLNDBN	Hermansky-Pudlak syndrome 4
Reversed	1
HGVS	NC_000022.10:g.26866740G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004344.1,

[PMID 23563589] An association study of the Hermansky-Pudlak syndrome type 4 gene in schizophrenic patients