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rs397508745

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508745(-;-)
Make rs397508745(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117534312
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508745
ebirs397508745
HLIrs397508745
Exacrs397508745
Varsomers397508745
Maprs397508745
PheGenIrs397508745
hapmaprs397508745
1000 genomesrs397508745
hgdprs397508745
ensemblrs397508745
gopubmedrs397508745
geneviewrs397508745
scholarrs397508745
googlers397508745
pharmgkbrs397508745
gwascentralrs397508745
openSNPrs397508745
23andMers397508745
23andMe allrs397508745
SNP Nexus

SNPshotrs397508745
SNPdbers397508745
MSV3drs397508745
GWAS Ctlgrs397508745
Max Magnitude0
ClinVar
Risk rs397508745(;)
Alt rs397508745(;)
Reference rs397508745(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117174366delA
CLNSRC ClinVar
CLNACC RCV000047178.2,