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rs1064794750

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome16
Position7333080
GeneRBFOX1
is asnp
is mentioned by
dbSNPrs1064794750
dbSNP (old)rs1064794750
ClinGenrs1064794750
ebirs1064794750
HLIrs1064794750
Exacrs1064794750
Gnomadrs1064794750
Varsomers1064794750
Maprs1064794750
PheGenIrs1064794750
Biobankrs1064794750
1000 genomesrs1064794750
hgdprs1064794750
ensemblrs1064794750
gopubmedrs1064794750
geneviewrs1064794750
scholarrs1064794750
googlers1064794750
pharmgkbrs1064794750
gwascentralrs1064794750
openSNPrs1064794750
23andMers1064794750
23andMe allrs1064794750
SNPshotrs1064794750
SNPdbers1064794750
MSV3drs1064794750
GWAS Ctlgrs1064794750
Max Magnitude0
ClinVar
Risk rs1064794750(G;G)
Alt rs1064794750(G;G)
Reference Rs1064794750(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RBFOX1
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.7383081C>G
CLNSRC
CLNACC RCV000484618.1,