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rs397508345

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508345(A;A)
Make rs397508345(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592323
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508345
ebirs397508345
HLIrs397508345
Exacrs397508345
Varsomers397508345
Maprs397508345
PheGenIrs397508345
hapmaprs397508345
1000 genomesrs397508345
hgdprs397508345
ensemblrs397508345
gopubmedrs397508345
geneviewrs397508345
scholarrs397508345
googlers397508345
pharmgkbrs397508345
gwascentralrs397508345
openSNPrs397508345
23andMers397508345
23andMe allrs397508345
SNP Nexus

SNPshotrs397508345
SNPdbers397508345
MSV3drs397508345
GWAS Ctlgrs397508345
Max Magnitude0
ClinVar
Risk rs397508345(A;A)
Alt rs397508345(A;A)
Reference rs397508345(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232377T>A
CLNSRC ClinVar
CLNACC RCV000046543.2,