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rs1057520670

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520670(C;G)
Make rs1057520670(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position173232767
GeneNKX2-5
is asnp
is mentioned by
dbSNPrs1057520670
dbSNP (classic)rs1057520670
ClinGenrs1057520670
ebirs1057520670
HLIrs1057520670
Exacrs1057520670
Gnomadrs1057520670
Varsomers1057520670
LitVarrs1057520670
Maprs1057520670
PheGenIrs1057520670
Biobankrs1057520670
1000 genomesrs1057520670
hgdprs1057520670
ensemblrs1057520670
geneviewrs1057520670
scholarrs1057520670
googlers1057520670
pharmgkbrs1057520670
gwascentralrs1057520670
openSNPrs1057520670
23andMers1057520670
23andMe allrs1057520670
SNPshotrs1057520670
SNPdbers1057520670
MSV3drs1057520670
GWAS Ctlgrs1057520670
Max Magnitude0
ClinVar
Risk rs1057520670(G;G)
Alt rs1057520670(G;G)
Reference Rs1057520670(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NKX2-5
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.172659770G>C
CLNSRC
CLNACC RCV000432384.1,