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rs397508739

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508739(-;-)
Make rs397508739(-;TT)
Make rs397508739(TT;TT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117480144
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508739
ebirs397508739
HLIrs397508739
Exacrs397508739
Varsomers397508739
Maprs397508739
PheGenIrs397508739
hapmaprs397508739
1000 genomesrs397508739
hgdprs397508739
ensemblrs397508739
gopubmedrs397508739
geneviewrs397508739
scholarrs397508739
googlers397508739
pharmgkbrs397508739
gwascentralrs397508739
openSNPrs397508739
23andMers397508739
23andMe allrs397508739
SNP Nexus

SNPshotrs397508739
SNPdbers397508739
MSV3drs397508739
GWAS Ctlgrs397508739
Max Magnitude0
ClinVar
Risk rs397508739(TT;TT)
Alt rs397508739(TT;TT)
Reference rs397508739(;)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117120197_117120198dupTT
CLNSRC ClinVar
CLNACC RCV000047170.3,