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rs878854423

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878854423(-;-)
Make rs878854423(-;C)
Make rs878854423(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position74743931
GeneKIAA2022
is asnp
is mentioned by
dbSNPrs878854423
ebirs878854423
HLIrs878854423
Exacrs878854423
Varsomers878854423
Maprs878854423
PheGenIrs878854423
hapmaprs878854423
1000 genomesrs878854423
hgdprs878854423
ensemblrs878854423
gopubmedrs878854423
geneviewrs878854423
scholarrs878854423
googlers878854423
pharmgkbrs878854423
gwascentralrs878854423
openSNPrs878854423
23andMers878854423
23andMe allrs878854423
SNP Nexus

SNPshotrs878854423
SNPdbers878854423
MSV3drs878854423
GWAS Ctlgrs878854423
Max Magnitude0
ClinVar
Risk rs878854423(C;C)
Alt rs878854423(C;C)
Reference rs878854423(;)
Significance Pathogenic
Disease not provided
Variation info
Gene KIAA2022
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.73963767dupG
CLNSRC
CLNACC RCV000231539.1,