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rs786204573

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204573(-;-)
Make rs786204573(-;A)
Make rs786204573(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position76346800
GeneBBS10
is asnp
is mentioned by
dbSNPrs786204573
ebirs786204573
HLIrs786204573
Exacrs786204573
Varsomers786204573
Maprs786204573
PheGenIrs786204573
hapmaprs786204573
1000 genomesrs786204573
hgdprs786204573
ensemblrs786204573
gopubmedrs786204573
geneviewrs786204573
scholarrs786204573
googlers786204573
pharmgkbrs786204573
gwascentralrs786204573
openSNPrs786204573
23andMers786204573
23andMe allrs786204573
SNP Nexus

SNPshotrs786204573
SNPdbers786204573
MSV3drs786204573
GWAS Ctlgrs786204573
Max Magnitude0
ClinVar
Risk rs786204573(A;A)
Alt rs786204573(A;A)
Reference rs786204573(;)
Significance Probable-Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 1
HGVS NC_000012.11:g.76740581dupT
CLNSRC
CLNACC RCV000169315.1,