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rs121909021

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 cystic fibrosis carrier
Make rs121909021(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540276
GeneCFTR
is asnp
is mentioned by
dbSNPrs121909021
ebirs121909021
HLIrs121909021
Exacrs121909021
Varsomers121909021
Maprs121909021
PheGenIrs121909021
hapmaprs121909021
1000 genomesrs121909021
hgdprs121909021
ensemblrs121909021
gopubmedrs121909021
geneviewrs121909021
scholarrs121909021
googlers121909021
pharmgkbrs121909021
gwascentralrs121909021
openSNPrs121909021
23andMers121909021
23andMe allrs121909021
SNP Nexus

SNPshotrs121909021
SNPdbers121909021
MSV3drs121909021
GWAS Ctlgrs121909021
Max Magnitude3
OMIM602421
Desc
Variant0068
Relatedalso
ClinVar
Risk rs121909021(T;T)
Alt rs121909021(T;T)
Reference rs121909021(C;C)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180330C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007592.3,