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rs121909031

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
(A;G) 3 cystic fibrosis carrier
Make rs121909031(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530951
GeneCFTR
is asnp
is mentioned by
dbSNPrs121909031
ebirs121909031
HLIrs121909031
Exacrs121909031
Varsomers121909031
Maprs121909031
PheGenIrs121909031
hapmaprs121909031
1000 genomesrs121909031
hgdprs121909031
ensemblrs121909031
gopubmedrs121909031
geneviewrs121909031
scholarrs121909031
googlers121909031
pharmgkbrs121909031
gwascentralrs121909031
openSNPrs121909031
23andMers121909031
23andMe allrs121909031
SNP Nexus

SNPshotrs121909031
SNPdbers121909031
MSV3drs121909031
GWAS Ctlgrs121909031
Max Magnitude3
OMIM602421
Desc
Variant0091
Relatedalso
ClinVar
Risk rs121909031(G;G)
Alt rs121909031(G;G)
Reference rs121909031(A;A)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171005A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007618.2,