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

rs397508306

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508306(A;T)
Make rs397508306(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117591968
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508306
ebirs397508306
HLIrs397508306
Exacrs397508306
Varsomers397508306
Maprs397508306
PheGenIrs397508306
hapmaprs397508306
1000 genomesrs397508306
hgdprs397508306
ensemblrs397508306
gopubmedrs397508306
geneviewrs397508306
scholarrs397508306
googlers397508306
pharmgkbrs397508306
gwascentralrs397508306
openSNPrs397508306
23andMers397508306
23andMe allrs397508306
SNP Nexus

SNPshotrs397508306
SNPdbers397508306
MSV3drs397508306
GWAS Ctlgrs397508306
Max Magnitude0
ClinVar
Risk rs397508306(T;T)
Alt rs397508306(T;T)
Reference rs397508306(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232022A>T
CLNSRC ClinVar
CLNACC RCV000046480.2,