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

rs397508530

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508530(-;-)
Make rs397508530(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530953
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508530
ebirs397508530
HLIrs397508530
Exacrs397508530
Varsomers397508530
Maprs397508530
PheGenIrs397508530
hapmaprs397508530
1000 genomesrs397508530
hgdprs397508530
ensemblrs397508530
gopubmedrs397508530
geneviewrs397508530
scholarrs397508530
googlers397508530
pharmgkbrs397508530
gwascentralrs397508530
openSNPrs397508530
23andMers397508530
23andMe allrs397508530
SNP Nexus

SNPshotrs397508530
SNPdbers397508530
MSV3drs397508530
GWAS Ctlgrs397508530
Max Magnitude0
ClinVar
Risk rs397508530(;)
Alt rs397508530(;)
Reference rs397508530(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171007delG
CLNSRC ClinVar
CLNACC RCV000046853.2,