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rs1064796882

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position74743791
GeneKIAA2022
is asnp
is mentioned by
dbSNPrs1064796882
dbSNP (old)rs1064796882
ClinGenrs1064796882
ebirs1064796882
HLIrs1064796882
Exacrs1064796882
Gnomadrs1064796882
Varsomers1064796882
Maprs1064796882
PheGenIrs1064796882
Biobankrs1064796882
1000 genomesrs1064796882
hgdprs1064796882
ensemblrs1064796882
gopubmedrs1064796882
geneviewrs1064796882
scholarrs1064796882
googlers1064796882
pharmgkbrs1064796882
gwascentralrs1064796882
openSNPrs1064796882
23andMers1064796882
23andMe allrs1064796882
SNPshotrs1064796882
SNPdbers1064796882
MSV3drs1064796882
GWAS Ctlgrs1064796882
Max Magnitude0
ClinVar
Risk rs1064796882(T;T)
Alt rs1064796882(T;T)
Reference Rs1064796882(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NEXMIF
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.73963626G>A
CLNSRC
CLNACC RCV000483441.1,