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rs121909037

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;C) 3 cystic fibrosis carrier
Make rs121909037(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611653
GeneCFTR
is asnp
is mentioned by
dbSNPrs121909037
ebirs121909037
HLIrs121909037
Exacrs121909037
Varsomers121909037
Maprs121909037
PheGenIrs121909037
hapmaprs121909037
1000 genomesrs121909037
hgdprs121909037
ensemblrs121909037
gopubmedrs121909037
geneviewrs121909037
scholarrs121909037
googlers121909037
pharmgkbrs121909037
gwascentralrs121909037
openSNPrs121909037
23andMers121909037
23andMe allrs121909037
SNP Nexus

SNPshotrs121909037
SNPdbers121909037
MSV3drs121909037
GWAS Ctlgrs121909037
Max Magnitude3
OMIM602421
Desc
Variant0104
Relatedalso
ClinVar
Risk rs121909037(C;C)
Alt rs121909037(C;C)
Reference rs121909037(A;A)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251707A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007630.3,