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rs587777422

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777422(-;-)
Make rs587777422(-;A)
Make rs587777422(A;A)
ReferenceGRCh38 38.1/142
Chromosome8
Position23702903
GeneNKX2-6
is asnp
is mentioned by
dbSNPrs587777422
ebirs587777422
HLIrs587777422
Exacrs587777422
Varsomers587777422
Maprs587777422
PheGenIrs587777422
hapmaprs587777422
1000 genomesrs587777422
hgdprs587777422
ensemblrs587777422
gopubmedrs587777422
geneviewrs587777422
scholarrs587777422
googlers587777422
pharmgkbrs587777422
gwascentralrs587777422
openSNPrs587777422
23andMers587777422
23andMe allrs587777422
SNP Nexus

SNPshotrs587777422
SNPdbers587777422
MSV3drs587777422
GWAS Ctlgrs587777422
Max Magnitude0
ClinVar
Risk rs587777422(A;A)
Alt rs587777422(A;A)
Reference rs587777422(;)
Significance Pathogenic
Disease Conotruncal heart malformations
Variation info
Gene NKX2-6
CLNDBN Conotruncal heart malformations
Reversed 1
HGVS NC_000008.10:g.23560416_23560417insA
CLNSRC OMIM Allelic Variant
CLNACC RCV000119845.2,