rs281865110

Orientation

minus

Stabilized

minus

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

Make rs281865110(A;A)

Make rs281865110(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

102066387

Gene

HPS6

is a	snp
is	mentioned by
dbSNP	rs281865110
dbSNP (classic)	rs281865110
ClinGen	rs281865110
ebi	rs281865110
HLI	rs281865110
Exac	rs281865110
Gnomad	rs281865110
Varsome	rs281865110
LitVar	rs281865110
Map	rs281865110
PheGenI	rs281865110
Biobank	rs281865110
1000 genomes	rs281865110
hgdp	rs281865110
ensembl	rs281865110
geneview	rs281865110
scholar	rs281865110
google	rs281865110
pharmgkb	rs281865110
gwascentral	rs281865110
openSNP	rs281865110
23andMe	rs281865110
SNPshot	rs281865110
SNPdbe	rs281865110
MSV3d	rs281865110
GWAS Ctlg	rs281865110

Max Magnitude

0

ClinVar
Risk	rs281865110(A;A)
Alt	rs281865110(A;A)
Reference	Rs281865110(G;G)
Significance	Pathogenic
Disease	Hermansky-Pudlak syndrome 6
Variation	info
Gene	HPS6
CLNDBN	Hermansky-Pudlak syndrome 6
Reversed	1
HGVS	NC_000010.10:g.103826144C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023650.3,