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rs121908754

From SNPedia

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


Make rs121908754(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117559643
GeneCFTR
is asnp
is mentioned by
dbSNPrs121908754
ebirs121908754
HLIrs121908754
Exacrs121908754
Varsomers121908754
Maprs121908754
PheGenIrs121908754
hapmaprs121908754
1000 genomesrs121908754
hgdprs121908754
ensemblrs121908754
gopubmedrs121908754
geneviewrs121908754
scholarrs121908754
googlers121908754
pharmgkbrs121908754
gwascentralrs121908754
openSNPrs121908754
23andMers121908754
23andMe allrs121908754
SNP Nexus

SNPshotrs121908754
SNPdbers121908754
MSV3drs121908754
GWAS Ctlgrs121908754
Merged fromRs121909014
Max Magnitude3
OMIM602421
Desc
Variant0047
Relatedalso
ClinVar
Risk rs121908754(A;A)
Alt rs121908754(A;A)
Reference rs121908754(C;C)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117199697C>A
CLNSRC CFTR2 OMIM Allelic Variant
CLNACC RCV000007571.3,