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rs121908771

From SNPedia

Cystic Fibrosis related
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;T) 3 cystic fibrosis carrier
(T;T) 0 common in clinvar


Make rs121908771(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117534317
GeneCFTR
is asnp
is mentioned by
dbSNPrs121908771
ebirs121908771
HLIrs121908771
Exacrs121908771
Varsomers121908771
Maprs121908771
PheGenIrs121908771
hapmaprs121908771
1000 genomesrs121908771
hgdprs121908771
ensemblrs121908771
gopubmedrs121908771
geneviewrs121908771
scholarrs121908771
googlers121908771
pharmgkbrs121908771
gwascentralrs121908771
openSNPrs121908771
23andMers121908771
23andMe allrs121908771
SNP Nexus

SNPshotrs121908771
SNPdbers121908771
MSV3drs121908771
GWAS Ctlgrs121908771
Max Magnitude3

Cystic fibrosis; c.531delT, Ile177Metfs

named i5010929 by 23andMe

ClinVar
Risk rs121908771(;)
Alt rs121908771(;)
Reference rs121908771(T;T)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117174371delT
CLNSRC CFTR2
CLNACC RCV000056393.3,