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rs397508740

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508740(C;T)
Make rs397508740(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117480098
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508740
ebirs397508740
HLIrs397508740
Exacrs397508740
Varsomers397508740
Maprs397508740
PheGenIrs397508740
hapmaprs397508740
1000 genomesrs397508740
hgdprs397508740
ensemblrs397508740
gopubmedrs397508740
geneviewrs397508740
scholarrs397508740
googlers397508740
pharmgkbrs397508740
gwascentralrs397508740
openSNPrs397508740
23andMers397508740
23andMe allrs397508740
SNP Nexus

SNPshotrs397508740
SNPdbers397508740
MSV3drs397508740
GWAS Ctlgrs397508740
Max Magnitude0
ClinVar
Risk rs397508740(T;T)
Alt rs397508740(T;T)
Reference rs397508740(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117120152C>T
CLNSRC ClinVar
CLNACC RCV000047171.2,