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rs869025206

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025206(-;-)
Make rs869025206(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position56514535
GeneBBS2
is asnp
is mentioned by
dbSNPrs869025206
ebirs869025206
HLIrs869025206
Exacrs869025206
Varsomers869025206
Maprs869025206
PheGenIrs869025206
hapmaprs869025206
1000 genomesrs869025206
hgdprs869025206
ensemblrs869025206
gopubmedrs869025206
geneviewrs869025206
scholarrs869025206
googlers869025206
pharmgkbrs869025206
gwascentralrs869025206
openSNPrs869025206
23andMers869025206
23andMe allrs869025206
SNP Nexus

SNPshotrs869025206
SNPdbers869025206
MSV3drs869025206
GWAS Ctlgrs869025206
Max Magnitude0
ClinVar
Risk rs869025206(;)
Alt rs869025206(;)
Reference rs869025206(G;G)
Significance Pathogenic
Disease Bardet-Biedl syndrome 2
Variation info
Gene BBS2
CLNDBN Bardet-Biedl syndrome 2
Reversed 1
HGVS NC_000016.9:g.56548447delC
CLNSRC
CLNACC RCV000207681.1,