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rs397508290

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508290(-;-)
Make rs397508290(-;T)
Make rs397508290(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117590412
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508290
ebirs397508290
HLIrs397508290
Exacrs397508290
Varsomers397508290
Maprs397508290
PheGenIrs397508290
hapmaprs397508290
1000 genomesrs397508290
hgdprs397508290
ensemblrs397508290
gopubmedrs397508290
geneviewrs397508290
scholarrs397508290
googlers397508290
pharmgkbrs397508290
gwascentralrs397508290
openSNPrs397508290
23andMers397508290
23andMe allrs397508290
SNP Nexus

SNPshotrs397508290
SNPdbers397508290
MSV3drs397508290
GWAS Ctlgrs397508290
Max Magnitude0
ClinVar
Risk rs397508290(T;T)
Alt rs397508290(T;T)
Reference rs397508290(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117230467dupT
CLNSRC ClinVar
CLNACC RCV000046453.2,