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rs786205498

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205498(A;A)
Make rs786205498(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position56510885
GeneBBS2
is asnp
is mentioned by
dbSNPrs786205498
ebirs786205498
HLIrs786205498
Exacrs786205498
Varsomers786205498
Maprs786205498
PheGenIrs786205498
hapmaprs786205498
1000 genomesrs786205498
hgdprs786205498
ensemblrs786205498
gopubmedrs786205498
geneviewrs786205498
scholarrs786205498
googlers786205498
pharmgkbrs786205498
gwascentralrs786205498
openSNPrs786205498
23andMers786205498
23andMe allrs786205498
SNP Nexus

SNPshotrs786205498
SNPdbers786205498
MSV3drs786205498
GWAS Ctlgrs786205498
Max Magnitude0
ClinVar
Risk rs786205498(A;A)
Alt rs786205498(A;A)
Reference rs786205498(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BBS2
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.56544797C>T
CLNSRC
CLNACC RCV000171247.1,