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rs121909009

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 cystic fibrosis carrier
Make rs121909009(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117548804
GeneCFTR
is asnp
is mentioned by
dbSNPrs121909009
ebirs121909009
HLIrs121909009
Exacrs121909009
Varsomers121909009
Maprs121909009
PheGenIrs121909009
hapmaprs121909009
1000 genomesrs121909009
hgdprs121909009
ensemblrs121909009
gopubmedrs121909009
geneviewrs121909009
scholarrs121909009
googlers121909009
pharmgkbrs121909009
gwascentralrs121909009
openSNPrs121909009
23andMers121909009
23andMe allrs121909009
SNP Nexus

SNPshotrs121909009
SNPdbers121909009
MSV3drs121909009
GWAS Ctlgrs121909009
Max Magnitude3
OMIM602421
Desc
Variant0028
Relatedalso
ClinVar
Risk rs121909009(T;T)
Alt rs121909009(T;T)
Reference rs121909009(G;G)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117188858G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007552.3,