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rs878854425

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854425(C;T)
Make rs878854425(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position74743620
GeneKIAA2022
is asnp
is mentioned by
dbSNPrs878854425
ebirs878854425
HLIrs878854425
Exacrs878854425
Varsomers878854425
Maprs878854425
PheGenIrs878854425
hapmaprs878854425
1000 genomesrs878854425
hgdprs878854425
ensemblrs878854425
gopubmedrs878854425
geneviewrs878854425
scholarrs878854425
googlers878854425
pharmgkbrs878854425
gwascentralrs878854425
openSNPrs878854425
23andMers878854425
23andMe allrs878854425
SNP Nexus

SNPshotrs878854425
SNPdbers878854425
MSV3drs878854425
GWAS Ctlgrs878854425
Max Magnitude0
ClinVar
Risk rs878854425(T;T)
Alt rs878854425(T;T)
Reference rs878854425(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KIAA2022
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.73963455G>A
CLNSRC
CLNACC RCV000229372.1,