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rs869312913

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312913(C;T)
Make rs869312913(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position72795832
GeneLOC105371339, ZFHX3
is asnp
is mentioned by
dbSNPrs869312913
ebirs869312913
HLIrs869312913
Exacrs869312913
Varsomers869312913
Maprs869312913
PheGenIrs869312913
hapmaprs869312913
1000 genomesrs869312913
hgdprs869312913
ensemblrs869312913
gopubmedrs869312913
geneviewrs869312913
scholarrs869312913
googlers869312913
pharmgkbrs869312913
gwascentralrs869312913
openSNPrs869312913
23andMers869312913
23andMe allrs869312913
SNP Nexus

SNPshotrs869312913
SNPdbers869312913
MSV3drs869312913
GWAS Ctlgrs869312913
Max Magnitude0
ClinVar
Risk rs869312913(T;T)
Alt rs869312913(T;T)
Reference rs869312913(C;C)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ZFHX3
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000016.9:g.72829731G>A
CLNSRC
CLNACC RCV000210628.1,