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rs397508343

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508343(C;T)
Make rs397508343(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592310
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508343
ebirs397508343
HLIrs397508343
Exacrs397508343
Varsomers397508343
Maprs397508343
PheGenIrs397508343
hapmaprs397508343
1000 genomesrs397508343
hgdprs397508343
ensemblrs397508343
gopubmedrs397508343
geneviewrs397508343
scholarrs397508343
googlers397508343
pharmgkbrs397508343
gwascentralrs397508343
openSNPrs397508343
23andMers397508343
23andMe allrs397508343
SNP Nexus

SNPshotrs397508343
SNPdbers397508343
MSV3drs397508343
GWAS Ctlgrs397508343
Max Magnitude0
ClinVar
Risk rs397508343(T;T)
Alt rs397508343(T;T)
Reference rs397508343(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232364C>T
CLNSRC ClinVar
CLNACC RCV000046541.2,