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

rs397508771

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508771(C;T)
Make rs397508771(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117535287
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508771
ebirs397508771
HLIrs397508771
Exacrs397508771
Varsomers397508771
Maprs397508771
PheGenIrs397508771
hapmaprs397508771
1000 genomesrs397508771
hgdprs397508771
ensemblrs397508771
gopubmedrs397508771
geneviewrs397508771
scholarrs397508771
googlers397508771
pharmgkbrs397508771
gwascentralrs397508771
openSNPrs397508771
23andMers397508771
23andMe allrs397508771
SNP Nexus

SNPshotrs397508771
SNPdbers397508771
MSV3drs397508771
GWAS Ctlgrs397508771
Max Magnitude0
ClinVar
Risk rs397508771(T;T)
Alt rs397508771(T;T)
Reference rs397508771(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117175341C>T
CLNSRC ClinVar
CLNACC RCV000047223.2,