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rs397508368

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508368(C;T)
Make rs397508368(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592508
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508368
ebirs397508368
HLIrs397508368
Exacrs397508368
Varsomers397508368
Maprs397508368
PheGenIrs397508368
hapmaprs397508368
1000 genomesrs397508368
hgdprs397508368
ensemblrs397508368
gopubmedrs397508368
geneviewrs397508368
scholarrs397508368
googlers397508368
pharmgkbrs397508368
gwascentralrs397508368
openSNPrs397508368
23andMers397508368
23andMe allrs397508368
SNP Nexus

SNPshotrs397508368
SNPdbers397508368
MSV3drs397508368
GWAS Ctlgrs397508368
Max Magnitude0
ClinVar
Risk rs397508368(T;T)
Alt rs397508368(T;T)
Reference rs397508368(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232562C>T
CLNSRC ClinVar
CLNACC RCV000046580.2,