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rs786204701

From SNPedia

Orientationplus
Geno Mag Summary
(CTTTG;CTTTG) 0 common in clinvar
Make rs786204701(-;-)
Make rs786204701(-;CTTTG)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position66526143
GeneBBS1, ZDHHC24
is asnp
is mentioned by
dbSNPrs786204701
ebirs786204701
HLIrs786204701
Exacrs786204701
Varsomers786204701
Maprs786204701
PheGenIrs786204701
hapmaprs786204701
1000 genomesrs786204701
hgdprs786204701
ensemblrs786204701
gopubmedrs786204701
geneviewrs786204701
scholarrs786204701
googlers786204701
pharmgkbrs786204701
gwascentralrs786204701
openSNPrs786204701
23andMers786204701
23andMe allrs786204701
SNP Nexus

SNPshotrs786204701
SNPdbers786204701
MSV3drs786204701
GWAS Ctlgrs786204701
Max Magnitude0
ClinVar
Risk rs786204701(;)
Alt rs786204701(;)
Reference rs786204701(CTTTG;CTTTG)
Significance Probable-Pathogenic
Disease Bardet-Biedl syndrome
Variation info
Gene BBS1 ZDHHC24
CLNDBN Bardet-Biedl syndrome
Reversed 0
HGVS NC_000011.9:g.66293614_66293618delCTTTG
CLNSRC Counsyl
CLNACC RCV000169515.1,