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rs786204705

From SNPedia

Orientationminus
Geno Mag Summary
(CTCAA;CTCAA) 0 common in clinvar
Make rs786204705(-;-)
Make rs786204705(-;CTCAA)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position76346533
GeneBBS10
is asnp
is mentioned by
dbSNPrs786204705
ebirs786204705
HLIrs786204705
Exacrs786204705
Varsomers786204705
Maprs786204705
PheGenIrs786204705
hapmaprs786204705
1000 genomesrs786204705
hgdprs786204705
ensemblrs786204705
gopubmedrs786204705
geneviewrs786204705
scholarrs786204705
googlers786204705
pharmgkbrs786204705
gwascentralrs786204705
openSNPrs786204705
23andMers786204705
23andMe allrs786204705
SNP Nexus

SNPshotrs786204705
SNPdbers786204705
MSV3drs786204705
GWAS Ctlgrs786204705
Max Magnitude0
ClinVar
Risk rs786204705(;)
Alt rs786204705(;)
Reference rs786204705(CTCAA;CTCAA)
Significance Probable-Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 1
HGVS NC_000012.11:g.76740313_76740317delTTGAG
CLNSRC Counsyl
CLNACC RCV000169519.1,