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rs397508794

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508794(-;-)
Make rs397508794(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117536577
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508794
ebirs397508794
HLIrs397508794
Exacrs397508794
Varsomers397508794
Maprs397508794
PheGenIrs397508794
hapmaprs397508794
1000 genomesrs397508794
hgdprs397508794
ensemblrs397508794
gopubmedrs397508794
geneviewrs397508794
scholarrs397508794
googlers397508794
pharmgkbrs397508794
gwascentralrs397508794
openSNPrs397508794
23andMers397508794
23andMe allrs397508794
SNP Nexus

SNPshotrs397508794
SNPdbers397508794
MSV3drs397508794
GWAS Ctlgrs397508794
Max Magnitude0
ClinVar
Risk rs397508794(;)
Alt rs397508794(;)
Reference rs397508794(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117176631delG
CLNSRC ClinVar
CLNACC RCV000047252.2,