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rs121909022

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;C) 3 cystic fibrosis carrier
(C;C) 0 common in clinvar


Make rs121909022(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117587815
GeneCFTR
is asnp
is mentioned by
dbSNPrs121909022
ebirs121909022
HLIrs121909022
Exacrs121909022
Varsomers121909022
Maprs121909022
PheGenIrs121909022
hapmaprs121909022
1000 genomesrs121909022
hgdprs121909022
ensemblrs121909022
gopubmedrs121909022
geneviewrs121909022
scholarrs121909022
googlers121909022
pharmgkbrs121909022
gwascentralrs121909022
openSNPrs121909022
23andMers121909022
23andMe allrs121909022
SNP Nexus

SNPshotrs121909022
SNPdbers121909022
MSV3drs121909022
GWAS Ctlgrs121909022
Max Magnitude3
OMIM602421
Desc
Variant0069
Relatedalso
ClinVar
Risk rs121909022(A;A)
Alt rs121909022(A;A)
Reference rs121909022(C;C)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117227869C>A
CLNSRC Cystic Fibrosis Mutation Database OMIM Allelic Variant
CLNACC RCV000007593.1,