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rs121909035

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 cystic fibrosis carrier
Make rs121909035(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117603719
GeneCFTR
is asnp
is mentioned by
dbSNPrs121909035
ebirs121909035
HLIrs121909035
Exacrs121909035
Varsomers121909035
Maprs121909035
PheGenIrs121909035
hapmaprs121909035
1000 genomesrs121909035
hgdprs121909035
ensemblrs121909035
gopubmedrs121909035
geneviewrs121909035
scholarrs121909035
googlers121909035
pharmgkbrs121909035
gwascentralrs121909035
openSNPrs121909035
23andMers121909035
23andMe allrs121909035
SNP Nexus

SNPshotrs121909035
SNPdbers121909035
MSV3drs121909035
GWAS Ctlgrs121909035
Max Magnitude3
OMIM602421
Desc
Variant0102
Relatedalso
ClinVar
Risk rs121909035(T;T)
Alt rs121909035(T;T)
Reference rs121909035(C;C)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117243773C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007628.3,