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rs104893678

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893678(C;T)
Make rs104893678(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position97788004
GeneARL6, LOC101929298
is asnp
is mentioned by
dbSNPrs104893678
ebirs104893678
HLIrs104893678
Exacrs104893678
Varsomers104893678
Maprs104893678
PheGenIrs104893678
hapmaprs104893678
1000 genomesrs104893678
hgdprs104893678
ensemblrs104893678
gopubmedrs104893678
geneviewrs104893678
scholarrs104893678
googlers104893678
pharmgkbrs104893678
gwascentralrs104893678
openSNPrs104893678
23andMers104893678
23andMe allrs104893678
SNP Nexus

SNPshotrs104893678
SNPdbers104893678
MSV3drs104893678
GWAS Ctlgrs104893678
Max Magnitude0
OMIM608845
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893678(T;T)
Alt rs104893678(T;T)
Reference rs104893678(C;C)
Significance Pathogenic
Disease Bardet-Biedl syndrome 3
Variation info
Gene ARL6 LOC101929298
CLNDBN Bardet-Biedl syndrome 3
Reversed 0
HGVS NC_000003.11:g.97506848C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002120.5,