Rs104893903

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Orientationminus
is asnp
is mentioned by
dbSNPrs104893903
PheGenIrs104893903
nextbiors104893903
hapmaprs104893903
1000 genomesrs104893903
hgdprs104893903
ensemblrs104893903
gopubmedrs104893903
geneviewrs104893903
scholarrs104893903
googlers104893903
pharmgkbrs104893903
gwascentralrs104893903
openSNPrs104893903
23andMers104893903
23andMe allrs104893903
SNP Nexus

SNPshotrs104893903
SNPdbers104893903
MSV3drs104893903
GeneNKX2-5
Chromosome5
Orientationminus
Position172659955
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893903(C;T)
Make rs104893903(T;T)
OMIM600584
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104893903(T;T)
Alt rs104893903(T;T)
Reference rs104893903(C;C)
Significance 5
Disease Atrial septal defect 7 with or without atrioventricular conduction defects
ClinVar info
Gene NKX2-5
CLNDBN Atrial septal defect 7 with or without atrioventricular conduction defects
Reversed 1
CLNHGVS NC_000005.9:g.172659955G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009570.3