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rs1057518152

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518152(A;A)
Make rs1057518152(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position13025553
GeneNFIX
is asnp
is mentioned by
dbSNPrs1057518152
dbSNP (old)rs1057518152
ClinGenrs1057518152
ebirs1057518152
HLIrs1057518152
Exacrs1057518152
Gnomadrs1057518152
Varsomers1057518152
Maprs1057518152
PheGenIrs1057518152
Biobankrs1057518152
1000 genomesrs1057518152
hgdprs1057518152
ensemblrs1057518152
gopubmedrs1057518152
geneviewrs1057518152
scholarrs1057518152
googlers1057518152
pharmgkbrs1057518152
gwascentralrs1057518152
openSNPrs1057518152
23andMers1057518152
23andMe allrs1057518152
SNPshotrs1057518152
SNPdbers1057518152
MSV3drs1057518152
GWAS Ctlgrs1057518152
Max Magnitude0
ClinVar
Risk rs1057518152(A;A)
Alt rs1057518152(A;A)
Reference Rs1057518152(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NFIX
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.13136367G>A
CLNSRC
CLNACC RCV000413514.1,