Have questions? Visit https://www.reddit.com/r/SNPedia

rs281865109

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865109(A;A)
Make rs281865109(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position102066289
GeneHPS6
is asnp
is mentioned by
dbSNPrs281865109
ebirs281865109
HLIrs281865109
Exacrs281865109
Varsomers281865109
Maprs281865109
PheGenIrs281865109
hapmaprs281865109
1000 genomesrs281865109
hgdprs281865109
ensemblrs281865109
gopubmedrs281865109
geneviewrs281865109
scholarrs281865109
googlers281865109
pharmgkbrs281865109
gwascentralrs281865109
openSNPrs281865109
23andMers281865109
23andMe allrs281865109
SNP Nexus

SNPshotrs281865109
SNPdbers281865109
MSV3drs281865109
GWAS Ctlgrs281865109
Max Magnitude0
ClinVar
Risk rs281865109(A;A)
Alt rs281865109(A;A)
Reference rs281865109(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.103826046C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023652.3,