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rs397508381

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508381(A;A)
Make rs397508381(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592643
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508381
ebirs397508381
HLIrs397508381
Exacrs397508381
Varsomers397508381
Maprs397508381
PheGenIrs397508381
hapmaprs397508381
1000 genomesrs397508381
hgdprs397508381
ensemblrs397508381
gopubmedrs397508381
geneviewrs397508381
scholarrs397508381
googlers397508381
pharmgkbrs397508381
gwascentralrs397508381
openSNPrs397508381
23andMers397508381
23andMe allrs397508381
SNP Nexus

SNPshotrs397508381
SNPdbers397508381
MSV3drs397508381
GWAS Ctlgrs397508381
Max Magnitude0
ClinVar
Risk rs397508381(A;A)
Alt rs397508381(A;A)
Reference rs397508381(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232697G>A
CLNSRC ClinVar
CLNACC RCV000046598.2,