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rs137854907

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137854907(C;C)
Make rs137854907(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position97784972
GeneARL6
is asnp
is mentioned by
dbSNPrs137854907
ClinGenrs137854907
ebirs137854907
HLIrs137854907
Exacrs137854907
Varsomers137854907
Maprs137854907
PheGenIrs137854907
hapmaprs137854907
1000 genomesrs137854907
hgdprs137854907
ensemblrs137854907
gopubmedrs137854907
geneviewrs137854907
scholarrs137854907
googlers137854907
pharmgkbrs137854907
gwascentralrs137854907
openSNPrs137854907
23andMers137854907
23andMe allrs137854907
SNP Nexus

SNPshotrs137854907
SNPdbers137854907
MSV3drs137854907
GWAS Ctlgrs137854907
Max Magnitude0
ClinVar
Risk rs137854907(C;C)
Alt rs137854907(C;C)
Reference Rs137854907(T;T)
Significance Pathogenic
Disease Bardet-Biedl syndrome
Variation info
Gene ARL6 LOC101929298
CLNDBN Bardet-Biedl syndrome
Reversed 0
HGVS NC_000003.11:g.97503816T>C
CLNSRC ClinVar
CLNACC RCV000058868.1,