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rs397508289

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508289(-;-)
Make rs397508289(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117590411
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508289
ebirs397508289
HLIrs397508289
Exacrs397508289
Varsomers397508289
Maprs397508289
PheGenIrs397508289
hapmaprs397508289
1000 genomesrs397508289
hgdprs397508289
ensemblrs397508289
gopubmedrs397508289
geneviewrs397508289
scholarrs397508289
googlers397508289
pharmgkbrs397508289
gwascentralrs397508289
openSNPrs397508289
23andMers397508289
23andMe allrs397508289
SNP Nexus

SNPshotrs397508289
SNPdbers397508289
MSV3drs397508289
GWAS Ctlgrs397508289
Max Magnitude0
ClinVar
Risk rs397508289(;)
Alt rs397508289(;)
Reference rs397508289(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117230465delG
CLNSRC ClinVar
CLNACC RCV000046452.2,