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rs370384522

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs370384522(A;A)
Make rs370384522(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position173366305
GeneCDCA7
is asnp
is mentioned by
dbSNPrs370384522
ebirs370384522
HLIrs370384522
Exacrs370384522
Varsomers370384522
Maprs370384522
PheGenIrs370384522
hapmaprs370384522
1000 genomesrs370384522
hgdprs370384522
ensemblrs370384522
gopubmedrs370384522
geneviewrs370384522
scholarrs370384522
googlers370384522
pharmgkbrs370384522
gwascentralrs370384522
openSNPrs370384522
23andMers370384522
23andMe allrs370384522
SNP Nexus

SNPshotrs370384522
SNPdbers370384522
MSV3drs370384522
GWAS Ctlgrs370384522
Max Magnitude0
ClinVar
Risk rs370384522(A;A)
Alt rs370384522(A;A)
Reference rs370384522(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.174231033G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000210914.1,