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rs121909025

From SNPedia

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


Make rs121909025(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117509040
GeneCFTR
is asnp
is mentioned by
dbSNPrs121909025
ebirs121909025
HLIrs121909025
Exacrs121909025
Varsomers121909025
Maprs121909025
PheGenIrs121909025
hapmaprs121909025
1000 genomesrs121909025
hgdprs121909025
ensemblrs121909025
gopubmedrs121909025
geneviewrs121909025
scholarrs121909025
googlers121909025
pharmgkbrs121909025
gwascentralrs121909025
openSNPrs121909025
23andMers121909025
23andMe allrs121909025
SNP Nexus

SNPshotrs121909025
SNPdbers121909025
MSV3drs121909025
GWAS Ctlgrs121909025
Max Magnitude3
OMIM602421
Desc
Variant0075
Relatedalso
ClinVar
Risk rs121909025(A;A)
Alt rs121909025(A;A)
Reference rs121909025(G;G)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117149094G>A
CLNSRC CFTR2 OMIM Allelic Variant
CLNACC RCV000007599.3,