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rs121909015

From SNPedia

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


Make rs121909015(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117642593
GeneCFTR
is asnp
is mentioned by
dbSNPrs121909015
ebirs121909015
HLIrs121909015
Exacrs121909015
Varsomers121909015
Maprs121909015
PheGenIrs121909015
hapmaprs121909015
1000 genomesrs121909015
hgdprs121909015
ensemblrs121909015
gopubmedrs121909015
geneviewrs121909015
scholarrs121909015
googlers121909015
pharmgkbrs121909015
gwascentralrs121909015
openSNPrs121909015
23andMers121909015
23andMe allrs121909015
SNP Nexus

SNPshotrs121909015
SNPdbers121909015
MSV3drs121909015
GWAS Ctlgrs121909015
Max Magnitude3
OMIM602421
Desc
Variant0048
Relatedalso
ClinVar
Risk rs121909015(C;C)
Alt rs121909015(C;C)
Reference rs121909015(G;G)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117282647G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007572.3,