Have questions? Visit https://www.reddit.com/r/SNPedia

rs869312972

From SNPedia

Orientationplus
Geno Mag Summary
(ACG;ACG) 0 common in clinvar
Make rs869312972(-;-)
Make rs869312972(-;ACG)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position74685487
GeneRORB
is asnp
is mentioned by
dbSNPrs869312972
ebirs869312972
HLIrs869312972
Exacrs869312972
Varsomers869312972
Maprs869312972
PheGenIrs869312972
hapmaprs869312972
1000 genomesrs869312972
hgdprs869312972
ensemblrs869312972
gopubmedrs869312972
geneviewrs869312972
scholarrs869312972
googlers869312972
pharmgkbrs869312972
gwascentralrs869312972
openSNPrs869312972
23andMers869312972
23andMe allrs869312972
SNP Nexus

SNPshotrs869312972
SNPdbers869312972
MSV3drs869312972
GWAS Ctlgrs869312972
Max Magnitude0
ClinVar
Risk rs869312972(;)
Alt rs869312972(;)
Reference rs869312972(ACG;ACG)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene RORB
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000009.11:g.77300403_77300405delACG
CLNSRC
CLNACC RCV000210738.1,