Have questions? Visit https://www.reddit.com/r/SNPedia

rs121908810

From SNPedia

Cystic Fibrosis related
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 cystic fibrosis carrier
Make rs121908810(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592457
GeneCFTR
is asnp
is mentioned by
dbSNPrs121908810
ebirs121908810
HLIrs121908810
Exacrs121908810
Varsomers121908810
Maprs121908810
PheGenIrs121908810
hapmaprs121908810
1000 genomesrs121908810
hgdprs121908810
ensemblrs121908810
gopubmedrs121908810
geneviewrs121908810
scholarrs121908810
googlers121908810
pharmgkbrs121908810
gwascentralrs121908810
openSNPrs121908810
23andMers121908810
23andMe allrs121908810
SNP Nexus

SNPshotrs121908810
SNPdbers121908810
MSV3drs121908810
GWAS Ctlgrs121908810
Max Magnitude3

Cystic fibrosis; c.2290C>T, p.Arg764Ter

named i5011532 by 23andMe

ClinVar
Risk rs121908810(T;T)
Alt rs121908810(T;T)
Reference rs121908810(C;C)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232511C>T
CLNSRC CFTR2
CLNACC RCV000056363.3,