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rs869312951

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312951(A;C)
Make rs869312951(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position26534508
GeneANO3
is asnp
is mentioned by
dbSNPrs869312951
ebirs869312951
HLIrs869312951
Exacrs869312951
Varsomers869312951
Maprs869312951
PheGenIrs869312951
hapmaprs869312951
1000 genomesrs869312951
hgdprs869312951
ensemblrs869312951
gopubmedrs869312951
geneviewrs869312951
scholarrs869312951
googlers869312951
pharmgkbrs869312951
gwascentralrs869312951
openSNPrs869312951
23andMers869312951
23andMe allrs869312951
SNP Nexus

SNPshotrs869312951
SNPdbers869312951
MSV3drs869312951
GWAS Ctlgrs869312951
Max Magnitude0
ClinVar
Risk rs869312951(C;C)
Alt rs869312951(C;C)
Reference rs869312951(A;A)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ANO3
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000011.9:g.26556055A>C
CLNSRC
CLNACC RCV000210588.1,