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

rs397508715

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508715(-;-)
Make rs397508715(-;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117480137
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508715
ebirs397508715
HLIrs397508715
Exacrs397508715
Varsomers397508715
Maprs397508715
PheGenIrs397508715
hapmaprs397508715
1000 genomesrs397508715
hgdprs397508715
ensemblrs397508715
gopubmedrs397508715
geneviewrs397508715
scholarrs397508715
googlers397508715
pharmgkbrs397508715
gwascentralrs397508715
openSNPrs397508715
23andMers397508715
23andMe allrs397508715
SNP Nexus

SNPshotrs397508715
SNPdbers397508715
MSV3drs397508715
GWAS Ctlgrs397508715
Max Magnitude0
ClinVar
Risk rs397508715(;)
Alt rs397508715(;)
Reference rs397508715(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117120191delC
CLNSRC ClinVar
CLNACC RCV000047133.2,