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rs397508809

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAAT;GAAT) 0 common in clinvar
Make rs397508809(-;-)
Make rs397508809(-;GAAT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117538987
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508809
ebirs397508809
HLIrs397508809
Exacrs397508809
Varsomers397508809
Maprs397508809
PheGenIrs397508809
hapmaprs397508809
1000 genomesrs397508809
hgdprs397508809
ensemblrs397508809
gopubmedrs397508809
geneviewrs397508809
scholarrs397508809
googlers397508809
pharmgkbrs397508809
gwascentralrs397508809
openSNPrs397508809
23andMers397508809
23andMe allrs397508809
SNP Nexus

SNPshotrs397508809
SNPdbers397508809
MSV3drs397508809
GWAS Ctlgrs397508809
Max Magnitude0
ClinVar
Risk rs397508809(;)
Alt rs397508809(;)
Reference rs397508809(GAAT;GAAT)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117179041_117179044delGAAT
CLNSRC ClinVar
CLNACC RCV000047275.2,