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rs1064796288

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Chromosome19
Position13025260
GeneNFIX
is asnp
is mentioned by
dbSNPrs1064796288
dbSNP (old)rs1064796288
ClinGenrs1064796288
ebirs1064796288
HLIrs1064796288
Exacrs1064796288
Gnomadrs1064796288
Varsomers1064796288
Maprs1064796288
PheGenIrs1064796288
Biobankrs1064796288
1000 genomesrs1064796288
hgdprs1064796288
ensemblrs1064796288
gopubmedrs1064796288
geneviewrs1064796288
scholarrs1064796288
googlers1064796288
pharmgkbrs1064796288
gwascentralrs1064796288
openSNPrs1064796288
23andMers1064796288
23andMe allrs1064796288
SNPshotrs1064796288
SNPdbers1064796288
MSV3drs1064796288
GWAS Ctlgrs1064796288
Max Magnitude0
ClinVar
Risk rs1064796288(C;C)
Alt rs1064796288(C;C)
Reference Rs1064796288(GG;GG)
Significance Pathogenic
Disease not provided
Variation info
Gene NFIX
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.13136074_13136075delGGinsC
CLNSRC
CLNACC RCV000480113.1,