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rs797044675

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044675(-;CC)
Make rs797044675(CC;CC)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position173232857
GeneNKX2-5
is asnp
is mentioned by
dbSNPrs797044675
dbSNP (old)rs797044675
ClinGenrs797044675
ebirs797044675
HLIrs797044675
Exacrs797044675
Gnomadrs797044675
Varsomers797044675
Maprs797044675
PheGenIrs797044675
Biobankrs797044675
1000 genomesrs797044675
hgdprs797044675
ensemblrs797044675
gopubmedrs797044675
geneviewrs797044675
scholarrs797044675
googlers797044675
pharmgkbrs797044675
gwascentralrs797044675
openSNPrs797044675
23andMers797044675
23andMe allrs797044675
SNP Nexus

SNPshotrs797044675
SNPdbers797044675
MSV3drs797044675
GWAS Ctlgrs797044675
Max Magnitude0
ClinVar
Risk rs797044675(CC;CC)
Alt rs797044675(CC;CC)
Reference Rs797044675(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene NKX2-5
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.172659860_172659861insGG
CLNSRC
CLNACC RCV000175778.1,