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rs878854418

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854418(-;-)
Make rs878854418(-;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position74744135
GeneKIAA2022
is asnp
is mentioned by
dbSNPrs878854418
ebirs878854418
HLIrs878854418
Exacrs878854418
Varsomers878854418
Maprs878854418
PheGenIrs878854418
hapmaprs878854418
1000 genomesrs878854418
hgdprs878854418
ensemblrs878854418
gopubmedrs878854418
geneviewrs878854418
scholarrs878854418
googlers878854418
pharmgkbrs878854418
gwascentralrs878854418
openSNPrs878854418
23andMers878854418
23andMe allrs878854418
SNP Nexus

SNPshotrs878854418
SNPdbers878854418
MSV3drs878854418
GWAS Ctlgrs878854418
Max Magnitude0
ClinVar
Risk rs878854418(;)
Alt rs878854418(;)
Reference rs878854418(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KIAA2022
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.73963970delT
CLNSRC
CLNACC RCV000230782.1,