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rs765715798

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs765715798(A;A)
Make rs765715798(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position97788002
GeneARL6
is asnp
is mentioned by
dbSNPrs765715798
ebirs765715798
HLIrs765715798
Exacrs765715798
Varsomers765715798
Maprs765715798
PheGenIrs765715798
hapmaprs765715798
1000 genomesrs765715798
hgdprs765715798
ensemblrs765715798
gopubmedrs765715798
geneviewrs765715798
scholarrs765715798
googlers765715798
pharmgkbrs765715798
gwascentralrs765715798
openSNPrs765715798
23andMers765715798
23andMe allrs765715798
SNP Nexus

SNPshotrs765715798
SNPdbers765715798
MSV3drs765715798
GWAS Ctlgrs765715798
Max Magnitude0
ClinVar
Risk rs765715798(A;A)
Alt rs765715798(A;A)
Reference rs765715798(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ARL6 LOC101929298
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.97506846G>A
CLNSRC
CLNACC RCV000171364.1,