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rs104893681

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104893681(G;G)
Make rs104893681(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position97791800
GeneARL6, LOC101929298
is asnp
is mentioned by
dbSNPrs104893681
ebirs104893681
HLIrs104893681
Exacrs104893681
Varsomers104893681
Maprs104893681
PheGenIrs104893681
hapmaprs104893681
1000 genomesrs104893681
hgdprs104893681
ensemblrs104893681
gopubmedrs104893681
geneviewrs104893681
scholarrs104893681
googlers104893681
pharmgkbrs104893681
gwascentralrs104893681
openSNPrs104893681
23andMers104893681
23andMe allrs104893681
SNP Nexus

SNPshotrs104893681
SNPdbers104893681
MSV3drs104893681
GWAS Ctlgrs104893681
Max Magnitude0
OMIM608845
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104893681(G;G)
Alt rs104893681(G;G)
Reference rs104893681(T;T)
Significance Pathogenic
Disease Bardet-Biedl syndrome 3
Variation info
Gene ARL6 LOC101929298
CLNDBN Bardet-Biedl syndrome 3
Reversed 0
HGVS NC_000003.11:g.97510644T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002124.3,