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rs786204671

From SNPedia

Orientationminus
Geno Mag Summary
(AAGA;AAGA) 0 common in clinvar
Make rs786204671(-;-)
Make rs786204671(-;AAGA)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position76347254
GeneBBS10
is asnp
is mentioned by
dbSNPrs786204671
ebirs786204671
HLIrs786204671
Exacrs786204671
Varsomers786204671
Maprs786204671
PheGenIrs786204671
hapmaprs786204671
1000 genomesrs786204671
hgdprs786204671
ensemblrs786204671
gopubmedrs786204671
geneviewrs786204671
scholarrs786204671
googlers786204671
pharmgkbrs786204671
gwascentralrs786204671
openSNPrs786204671
23andMers786204671
23andMe allrs786204671
SNP Nexus

SNPshotrs786204671
SNPdbers786204671
MSV3drs786204671
GWAS Ctlgrs786204671
Max Magnitude0
ClinVar
Risk rs786204671(;)
Alt rs786204671(;)
Reference rs786204671(AAGA;AAGA)
Significance Probable-Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 1
HGVS NC_000012.11:g.76741034_76741037delTCTT
CLNSRC
CLNACC RCV000169474.1,