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rs876657409

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657409(-;-)
Make rs876657409(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position173366365
GeneCDCA7
is asnp
is mentioned by
dbSNPrs876657409
ebirs876657409
HLIrs876657409
Exacrs876657409
Varsomers876657409
Maprs876657409
PheGenIrs876657409
hapmaprs876657409
1000 genomesrs876657409
hgdprs876657409
ensemblrs876657409
gopubmedrs876657409
geneviewrs876657409
scholarrs876657409
googlers876657409
pharmgkbrs876657409
gwascentralrs876657409
openSNPrs876657409
23andMers876657409
23andMe allrs876657409
SNP Nexus

SNPshotrs876657409
SNPdbers876657409
MSV3drs876657409
GWAS Ctlgrs876657409
Max Magnitude0
ClinVar
Risk rs876657409(;)
Alt rs876657409(;)
Reference rs876657409(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.174231093delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000210916.1,