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rs201196733

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201196733(A;A)
Make rs201196733(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position56497013
GeneBBS2
is asnp
is mentioned by
dbSNPrs201196733
dbSNP (old)rs201196733
ClinGenrs201196733
ebirs201196733
HLIrs201196733
Exacrs201196733
Gnomadrs201196733
Varsomers201196733
LitVarrs201196733
Maprs201196733
PheGenIrs201196733
Biobankrs201196733
1000 genomesrs201196733
hgdprs201196733
ensemblrs201196733
gopubmedrs201196733
geneviewrs201196733
scholarrs201196733
googlers201196733
pharmgkbrs201196733
gwascentralrs201196733
openSNPrs201196733
23andMers201196733
23andMe allrs201196733
SNPshotrs201196733
SNPdbers201196733
MSV3drs201196733
GWAS Ctlgrs201196733
Max Magnitude0
ClinVar
Risk rs201196733(A;A) rs201196733(C;C)
Alt rs201196733(A;A) rs201196733(C;C)
Reference Rs201196733(G;G)
Significance Other
Disease Bardet-Biedl syndrome 2 not provided
Variation info
Gene BBS2
CLNDBN Bardet-Biedl syndrome 2 not provided
Reversed 0
HGVS NC_000016.9:g.56530925G>A
CLNSRC
CLNACC RCV000335732.1, RCV000424669.1,