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rs772929976

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs772929976(A;A)
Make rs772929976(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position173366395
GeneCDCA7
is asnp
is mentioned by
dbSNPrs772929976
ebirs772929976
HLIrs772929976
Exacrs772929976
Varsomers772929976
Maprs772929976
PheGenIrs772929976
hapmaprs772929976
1000 genomesrs772929976
hgdprs772929976
ensemblrs772929976
gopubmedrs772929976
geneviewrs772929976
scholarrs772929976
googlers772929976
pharmgkbrs772929976
gwascentralrs772929976
openSNPrs772929976
23andMers772929976
23andMe allrs772929976
SNP Nexus

SNPshotrs772929976
SNPdbers772929976
MSV3drs772929976
GWAS Ctlgrs772929976
Max Magnitude0
ClinVar
Risk rs772929976(A;A)
Alt rs772929976(A;A)
Reference rs772929976(G;G)
Significance Pathogenic
Disease Immunodeficiency-centromeric instability-facial anomalies syndrome 3
Variation info
Gene CDCA7
CLNDBN Immunodeficiency-centromeric instability-facial anomalies syndrome 3
Reversed 0
HGVS NC_000002.11:g.174231123G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000210909.1,