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rs753966933

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs753966933(A;A)
Make rs753966933(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position55228708
GeneRAB27A
is asnp
is mentioned by
dbSNPrs753966933
dbSNP (classic)rs753966933
ClinGenrs753966933
ebirs753966933
HLIrs753966933
Exacrs753966933
Gnomadrs753966933
Varsomers753966933
LitVarrs753966933
Maprs753966933
PheGenIrs753966933
Biobankrs753966933
1000 genomesrs753966933
hgdprs753966933
ensemblrs753966933
geneviewrs753966933
scholarrs753966933
googlers753966933
pharmgkbrs753966933
gwascentralrs753966933
openSNPrs753966933
23andMers753966933
SNPshotrs753966933
SNPdbers753966933
MSV3drs753966933
GWAS Ctlgrs753966933
Max Magnitude0
ClinVar
Risk rs753966933(A;A)
Alt rs753966933(A;A)
Reference Rs753966933(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAB27A
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.55520906G>A
CLNSRC
CLNACC RCV000483557.1,