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rs397508333

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508333(A;A)
Make rs397508333(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592203
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508333
ebirs397508333
HLIrs397508333
Exacrs397508333
Varsomers397508333
Maprs397508333
PheGenIrs397508333
hapmaprs397508333
1000 genomesrs397508333
hgdprs397508333
ensemblrs397508333
gopubmedrs397508333
geneviewrs397508333
scholarrs397508333
googlers397508333
pharmgkbrs397508333
gwascentralrs397508333
openSNPrs397508333
23andMers397508333
23andMe allrs397508333
SNP Nexus

SNPshotrs397508333
SNPdbers397508333
MSV3drs397508333
GWAS Ctlgrs397508333
Max Magnitude0
ClinVar
Risk rs397508333(A;A)
Alt rs397508333(A;A)
Reference rs397508333(G;G)
Significance Probable-Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232257G>A
CLNSRC ClinVar
CLNACC RCV000046525.3,