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rs749974697

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs749974697(C;T)
Make rs749974697(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position33152851
GeneBBS9
is asnp
is mentioned by
dbSNPrs749974697
ebirs749974697
HLIrs749974697
Exacrs749974697
Varsomers749974697
Maprs749974697
PheGenIrs749974697
hapmaprs749974697
1000 genomesrs749974697
hgdprs749974697
ensemblrs749974697
gopubmedrs749974697
geneviewrs749974697
scholarrs749974697
googlers749974697
pharmgkbrs749974697
gwascentralrs749974697
openSNPrs749974697
23andMers749974697
23andMe allrs749974697
SNP Nexus

SNPshotrs749974697
SNPdbers749974697
MSV3drs749974697
GWAS Ctlgrs749974697
Max Magnitude0
ClinVar
Risk rs749974697(T;T)
Alt rs749974697(T;T)
Reference rs749974697(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BBS9
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.33192463C>A
CLNSRC
CLNACC RCV000171406.1,