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

rs397508552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs397508552(AC;GTA)
Make rs397508552(GTA;GTA)
ReferenceGRCh38 38.1/141
Chromosome7
Position117614645
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508552
ebirs397508552
HLIrs397508552
Exacrs397508552
Varsomers397508552
Maprs397508552
PheGenIrs397508552
hapmaprs397508552
1000 genomesrs397508552
hgdprs397508552
ensemblrs397508552
gopubmedrs397508552
geneviewrs397508552
scholarrs397508552
googlers397508552
pharmgkbrs397508552
gwascentralrs397508552
openSNPrs397508552
23andMers397508552
23andMe allrs397508552
SNP Nexus

SNPshotrs397508552
SNPdbers397508552
MSV3drs397508552
GWAS Ctlgrs397508552
Max Magnitude0
ClinVar
Risk rs397508552(GTA;GTA)
Alt rs397508552(GTA;GTA)
Reference rs397508552(AC;AC)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117254699_117254700delACinsGTA
CLNSRC ClinVar
CLNACC RCV000046880.2,