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rs397508382

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508382(A;T)
Make rs397508382(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592655
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508382
ebirs397508382
HLIrs397508382
Exacrs397508382
Varsomers397508382
Maprs397508382
PheGenIrs397508382
hapmaprs397508382
1000 genomesrs397508382
hgdprs397508382
ensemblrs397508382
gopubmedrs397508382
geneviewrs397508382
scholarrs397508382
googlers397508382
pharmgkbrs397508382
gwascentralrs397508382
openSNPrs397508382
23andMers397508382
23andMe allrs397508382
SNP Nexus

SNPshotrs397508382
SNPdbers397508382
MSV3drs397508382
GWAS Ctlgrs397508382
Max Magnitude0
ClinVar
Risk rs397508382(T;T)
Alt rs397508382(T;T)
Reference rs397508382(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232709A>T
CLNSRC ClinVar
CLNACC RCV000046600.2,