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rs104893679

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893679(C;C)
Make rs104893679(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position97791797
GeneARL6, LOC101929298
is asnp
is mentioned by
dbSNPrs104893679
ebirs104893679
HLIrs104893679
Exacrs104893679
Varsomers104893679
Maprs104893679
PheGenIrs104893679
hapmaprs104893679
1000 genomesrs104893679
hgdprs104893679
ensemblrs104893679
gopubmedrs104893679
geneviewrs104893679
scholarrs104893679
googlers104893679
pharmgkbrs104893679
gwascentralrs104893679
openSNPrs104893679
23andMers104893679
23andMe allrs104893679
SNP Nexus

SNPshotrs104893679
SNPdbers104893679
MSV3drs104893679
GWAS Ctlgrs104893679
Max Magnitude0
OMIM608845
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104893679(C;C)
Alt rs104893679(C;C)
Reference rs104893679(G;G)
Significance Other
Disease Bardet-Biedl syndrome 3 Bardet-Biedl syndrome 1
Variation info
Gene ARL6 LOC101929298
CLNDBN Bardet-Biedl syndrome 3 Bardet-Biedl syndrome 1, modifier of
Reversed 0
HGVS NC_000003.11:g.97510641G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002121.3, RCV000002122.4,