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rs397508389

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508389(-;-)
Make rs397508389(-;T)
Make rs397508389(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117594941
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508389
ebirs397508389
HLIrs397508389
Exacrs397508389
Varsomers397508389
Maprs397508389
PheGenIrs397508389
hapmaprs397508389
1000 genomesrs397508389
hgdprs397508389
ensemblrs397508389
gopubmedrs397508389
geneviewrs397508389
scholarrs397508389
googlers397508389
pharmgkbrs397508389
gwascentralrs397508389
openSNPrs397508389
23andMers397508389
23andMe allrs397508389
SNP Nexus

SNPshotrs397508389
SNPdbers397508389
MSV3drs397508389
GWAS Ctlgrs397508389
Max Magnitude0
ClinVar
Risk rs397508389(T;T)
Alt rs397508389(T;T)
Reference rs397508389(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117234995dupT
CLNSRC ClinVar
CLNACC RCV000046608.2,