rs281865099

Orientation

minus

Stabilized

minus

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

Make rs281865099(-;-)

Make rs281865099(-;C)

Reference

GRCh38 38.1/141

Chromosome

22

Position

26457948

Gene

HPS4

is a	snp
is	mentioned by
dbSNP	rs281865099
dbSNP (classic)	rs281865099
ClinGen	rs281865099
ebi	rs281865099
HLI	rs281865099
Exac	rs281865099
Gnomad	rs281865099
Varsome	rs281865099
LitVar	rs281865099
Map	rs281865099
PheGenI	rs281865099
Biobank	rs281865099
1000 genomes	rs281865099
hgdp	rs281865099
ensembl	rs281865099
geneview	rs281865099
scholar	rs281865099
google	rs281865099
pharmgkb	rs281865099
gwascentral	rs281865099
openSNP	rs281865099
23andMe	rs281865099
SNPshot	rs281865099
SNPdbe	rs281865099
MSV3d	rs281865099
GWAS Ctlg	rs281865099

Max Magnitude

0

ClinVar
Risk	rs281865099(-;-)
Alt	rs281865099(-;-)
Reference	Rs281865099(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.26853914delG
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020868.1,