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rs397508365

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508365(C;G)
Make rs397508365(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592494
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508365
ebirs397508365
HLIrs397508365
Exacrs397508365
Varsomers397508365
Maprs397508365
PheGenIrs397508365
hapmaprs397508365
1000 genomesrs397508365
hgdprs397508365
ensemblrs397508365
gopubmedrs397508365
geneviewrs397508365
scholarrs397508365
googlers397508365
pharmgkbrs397508365
gwascentralrs397508365
openSNPrs397508365
23andMers397508365
23andMe allrs397508365
SNP Nexus

SNPshotrs397508365
SNPdbers397508365
MSV3drs397508365
GWAS Ctlgrs397508365
Max Magnitude0
ClinVar
Risk rs397508365(G;G)
Alt rs397508365(G;G)
Reference rs397508365(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232548C>G
CLNSRC ClinVar
CLNACC RCV000046576.2,