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rs179363897

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs179363897(A;A)
Make rs179363897(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position169492900
GeneBBS5
is asnp
is mentioned by
dbSNPrs179363897
ebirs179363897
HLIrs179363897
Exacrs179363897
Varsomers179363897
Maprs179363897
PheGenIrs179363897
hapmaprs179363897
1000 genomesrs179363897
hgdprs179363897
ensemblrs179363897
gopubmedrs179363897
geneviewrs179363897
scholarrs179363897
googlers179363897
pharmgkbrs179363897
gwascentralrs179363897
openSNPrs179363897
23andMers179363897
23andMe allrs179363897
SNP Nexus

SNPshotrs179363897
SNPdbers179363897
MSV3drs179363897
GWAS Ctlgrs179363897
Max Magnitude0
ClinVar
Risk rs179363897(A;A)
Alt rs179363897(A;A)
Reference rs179363897(G;G)
Significance Pathogenic
Disease Bardet-Biedl syndrome
Variation info
Gene BBS5
CLNDBN Bardet-Biedl syndrome
Reversed 0
HGVS NC_000002.11:g.170349410G>A
CLNSRC ClinVar
CLNACC RCV000058870.1,