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rs869312971

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312971(C;C)
Make rs869312971(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position74634755
GeneLOC105376088, RORB
is asnp
is mentioned by
dbSNPrs869312971
ebirs869312971
HLIrs869312971
Exacrs869312971
Varsomers869312971
Maprs869312971
PheGenIrs869312971
hapmaprs869312971
1000 genomesrs869312971
hgdprs869312971
ensemblrs869312971
gopubmedrs869312971
geneviewrs869312971
scholarrs869312971
googlers869312971
pharmgkbrs869312971
gwascentralrs869312971
openSNPrs869312971
23andMers869312971
23andMe allrs869312971
SNP Nexus

SNPshotrs869312971
SNPdbers869312971
MSV3drs869312971
GWAS Ctlgrs869312971
Max Magnitude0
ClinVar
Risk rs869312971(C;C)
Alt rs869312971(C;C)
Reference rs869312971(T;T)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene RORB
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000009.11:g.77249671T>C
CLNSRC
CLNACC RCV000210680.1,