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rs786205826

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205826(-;-)
Make rs786205826(-;C)
Make rs786205826(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position173232989
GeneNKX2-5
is asnp
is mentioned by
dbSNPrs786205826
ebirs786205826
HLIrs786205826
Exacrs786205826
Varsomers786205826
Maprs786205826
PheGenIrs786205826
hapmaprs786205826
1000 genomesrs786205826
hgdprs786205826
ensemblrs786205826
gopubmedrs786205826
geneviewrs786205826
scholarrs786205826
googlers786205826
pharmgkbrs786205826
gwascentralrs786205826
openSNPrs786205826
23andMers786205826
23andMe allrs786205826
SNP Nexus

SNPshotrs786205826
SNPdbers786205826
MSV3drs786205826
GWAS Ctlgrs786205826
Max Magnitude0
ClinVar
Risk rs786205826(C;C)
Alt rs786205826(C;C)
Reference rs786205826(;)
Significance Pathogenic
Disease not provided
Variation info
Gene NKX2-5
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.172659992_172659993insG
CLNSRC
CLNACC RCV000171016.2,