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rs397508798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508798(-;-)
Make rs397508798(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117504279
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508798
ebirs397508798
HLIrs397508798
Exacrs397508798
Varsomers397508798
Maprs397508798
PheGenIrs397508798
hapmaprs397508798
1000 genomesrs397508798
hgdprs397508798
ensemblrs397508798
gopubmedrs397508798
geneviewrs397508798
scholarrs397508798
googlers397508798
pharmgkbrs397508798
gwascentralrs397508798
openSNPrs397508798
23andMers397508798
23andMe allrs397508798
SNP Nexus

SNPshotrs397508798
SNPdbers397508798
MSV3drs397508798
GWAS Ctlgrs397508798
Max Magnitude0
ClinVar
Risk rs397508798(;)
Alt rs397508798(;)
Reference rs397508798(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117144333delG
CLNSRC ClinVar
CLNACC RCV000047261.2,