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

rs397508274

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508274(-;-)
Make rs397508274(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117590376
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508274
ebirs397508274
HLIrs397508274
Exacrs397508274
Varsomers397508274
Maprs397508274
PheGenIrs397508274
hapmaprs397508274
1000 genomesrs397508274
hgdprs397508274
ensemblrs397508274
gopubmedrs397508274
geneviewrs397508274
scholarrs397508274
googlers397508274
pharmgkbrs397508274
gwascentralrs397508274
openSNPrs397508274
23andMers397508274
23andMe allrs397508274
SNP Nexus

SNPshotrs397508274
SNPdbers397508274
MSV3drs397508274
GWAS Ctlgrs397508274
Max Magnitude0
ClinVar
Risk rs397508274(;)
Alt rs397508274(;)
Reference rs397508274(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117230430delT
CLNSRC ClinVar
CLNACC RCV000046431.2,