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rs121909033

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 3 cystic fibrosis carrier
Make rs121909033(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592110
GeneCFTR
is asnp
is mentioned by
dbSNPrs121909033
ebirs121909033
HLIrs121909033
Exacrs121909033
Varsomers121909033
Maprs121909033
PheGenIrs121909033
hapmaprs121909033
1000 genomesrs121909033
hgdprs121909033
ensemblrs121909033
gopubmedrs121909033
geneviewrs121909033
scholarrs121909033
googlers121909033
pharmgkbrs121909033
gwascentralrs121909033
openSNPrs121909033
23andMers121909033
23andMe allrs121909033
SNP Nexus

SNPshotrs121909033
SNPdbers121909033
MSV3drs121909033
GWAS Ctlgrs121909033
Max Magnitude3
OMIM602421
Desc
Variant0097
Relatedalso
ClinVar
Risk rs121909033(T;T)
Alt rs121909033(T;T)
Reference rs121909033(A;A)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232164A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007623.3,