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rs281865110

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865110(A;A)
Make rs281865110(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position102066387
GeneHPS6
is asnp
is mentioned by
dbSNPrs281865110
ebirs281865110
HLIrs281865110
Exacrs281865110
Varsomers281865110
Maprs281865110
PheGenIrs281865110
hapmaprs281865110
1000 genomesrs281865110
hgdprs281865110
ensemblrs281865110
gopubmedrs281865110
geneviewrs281865110
scholarrs281865110
googlers281865110
pharmgkbrs281865110
gwascentralrs281865110
openSNPrs281865110
23andMers281865110
23andMe allrs281865110
SNP Nexus

SNPshotrs281865110
SNPdbers281865110
MSV3drs281865110
GWAS Ctlgrs281865110
Max Magnitude0
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,