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rs121909028

From SNPedia

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


Make rs121909028(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117642577
GeneCFTR
is asnp
is mentioned by
dbSNPrs121909028
ebirs121909028
HLIrs121909028
Exacrs121909028
Varsomers121909028
Maprs121909028
PheGenIrs121909028
hapmaprs121909028
1000 genomesrs121909028
hgdprs121909028
ensemblrs121909028
gopubmedrs121909028
geneviewrs121909028
scholarrs121909028
googlers121909028
pharmgkbrs121909028
gwascentralrs121909028
openSNPrs121909028
23andMers121909028
23andMe allrs121909028
SNP Nexus

SNPshotrs121909028
SNPdbers121909028
MSV3drs121909028
GWAS Ctlgrs121909028
Max Magnitude3
OMIM602421
Desc
Variant0080
Relatedalso
ClinVar
Risk rs121909028(C;C)
Alt rs121909028(C;C)
Reference rs121909028(T;T)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117282631T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007604.3,