Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519223

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519223(C;T)
Make rs1057519223(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position36517612
GeneNKX2-1, NKX2-1-AS1, SFTA3
is asnp
is mentioned by
dbSNPrs1057519223
dbSNP (old)rs1057519223
ClinGenrs1057519223
ebirs1057519223
HLIrs1057519223
Exacrs1057519223
Gnomadrs1057519223
Varsomers1057519223
LitVarrs1057519223
Maprs1057519223
PheGenIrs1057519223
Biobankrs1057519223
1000 genomesrs1057519223
hgdprs1057519223
ensemblrs1057519223
gopubmedrs1057519223
geneviewrs1057519223
scholarrs1057519223
googlers1057519223
pharmgkbrs1057519223
gwascentralrs1057519223
openSNPrs1057519223
23andMers1057519223
23andMe allrs1057519223
SNPshotrs1057519223
SNPdbers1057519223
MSV3drs1057519223
GWAS Ctlgrs1057519223
Max Magnitude0
ClinVar
Risk rs1057519223(T;T)
Alt rs1057519223(T;T)
Reference Rs1057519223(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NKX2-1-AS1 SFTA3 NKX2-1
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.36986817G>A
CLNSRC
CLNACC RCV000415944.2,