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rs397508167

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508167(-;-)
Make rs397508167(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117542051
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508167
ebirs397508167
HLIrs397508167
Exacrs397508167
Varsomers397508167
Maprs397508167
PheGenIrs397508167
hapmaprs397508167
1000 genomesrs397508167
hgdprs397508167
ensemblrs397508167
gopubmedrs397508167
geneviewrs397508167
scholarrs397508167
googlers397508167
pharmgkbrs397508167
gwascentralrs397508167
openSNPrs397508167
23andMers397508167
23andMe allrs397508167
SNP Nexus

SNPshotrs397508167
SNPdbers397508167
MSV3drs397508167
GWAS Ctlgrs397508167
Max Magnitude0
ClinVar
Risk rs397508167(;)
Alt rs397508167(;)
Reference rs397508167(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117182105delA
CLNSRC ClinVar
CLNACC RCV000046246.2,