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rs1085307714

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome19
Position13081681
GeneNFIX
is asnp
is mentioned by
dbSNPrs1085307714
dbSNP (old)rs1085307714
ClinGenrs1085307714
ebirs1085307714
HLIrs1085307714
Exacrs1085307714
Gnomadrs1085307714
Varsomers1085307714
Maprs1085307714
PheGenIrs1085307714
Biobankrs1085307714
1000 genomesrs1085307714
hgdprs1085307714
ensemblrs1085307714
gopubmedrs1085307714
geneviewrs1085307714
scholarrs1085307714
googlers1085307714
pharmgkbrs1085307714
gwascentralrs1085307714
openSNPrs1085307714
23andMers1085307714
23andMe allrs1085307714
SNPshotrs1085307714
SNPdbers1085307714
MSV3drs1085307714
GWAS Ctlgrs1085307714
Max Magnitude0
ClinVar
Risk rs1085307714(-;-)
Alt rs1085307714(-;-)
Reference Rs1085307714(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NFIX
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.13192495delG
CLNSRC
CLNACC RCV000489396.1,