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rs786205824

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205824(C;C)
Make rs786205824(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position173232978
GeneNKX2-5
is asnp
is mentioned by
dbSNPrs786205824
ebirs786205824
HLIrs786205824
Exacrs786205824
Varsomers786205824
Maprs786205824
PheGenIrs786205824
hapmaprs786205824
1000 genomesrs786205824
hgdprs786205824
ensemblrs786205824
gopubmedrs786205824
geneviewrs786205824
scholarrs786205824
googlers786205824
pharmgkbrs786205824
gwascentralrs786205824
openSNPrs786205824
23andMers786205824
23andMe allrs786205824
SNP Nexus

SNPshotrs786205824
SNPdbers786205824
MSV3drs786205824
GWAS Ctlgrs786205824
Max Magnitude0
ClinVar
Risk rs786205824(C;C)
Alt rs786205824(C;C)
Reference rs786205824(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NKX2-5
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.172659981C>G
CLNSRC
CLNACC RCV000171010.3,