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rs281865107

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865107(A;A)
Make rs281865107(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position102065697
GeneHPS6
is asnp
is mentioned by
dbSNPrs281865107
ebirs281865107
HLIrs281865107
Exacrs281865107
Varsomers281865107
Maprs281865107
PheGenIrs281865107
hapmaprs281865107
1000 genomesrs281865107
hgdprs281865107
ensemblrs281865107
gopubmedrs281865107
geneviewrs281865107
scholarrs281865107
googlers281865107
pharmgkbrs281865107
gwascentralrs281865107
openSNPrs281865107
23andMers281865107
23andMe allrs281865107
SNP Nexus

SNPshotrs281865107
SNPdbers281865107
MSV3drs281865107
GWAS Ctlgrs281865107
Max Magnitude0
ClinVar
Risk rs281865107(A;A)
Alt rs281865107(A;A)
Reference rs281865107(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.103825454C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023653.3,