rs281865112

Orientation

minus

Stabilized

minus

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

Make rs281865112(A;A)

Make rs281865112(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

102066708

Gene

HPS6

is a	snp
is	mentioned by
dbSNP	rs281865112
dbSNP (classic)	rs281865112
ClinGen	rs281865112
ebi	rs281865112
HLI	rs281865112
Exac	rs281865112
Gnomad	rs281865112
Varsome	rs281865112
LitVar	rs281865112
Map	rs281865112
PheGenI	rs281865112
Biobank	rs281865112
1000 genomes	rs281865112
hgdp	rs281865112
ensembl	rs281865112
geneview	rs281865112
scholar	rs281865112
google	rs281865112
pharmgkb	rs281865112
gwascentral	rs281865112
openSNP	rs281865112
23andMe	rs281865112
SNPshot	rs281865112
SNPdbe	rs281865112
MSV3d	rs281865112
GWAS Ctlg	rs281865112

Max Magnitude

0

ClinVar
Risk	rs281865112(A;A)
Alt	rs281865112(A;A)
Reference	Rs281865112(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.103826465C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023654.4,