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rs397508434

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508434(-;-)
Make rs397508434(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117603651
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508434
ebirs397508434
HLIrs397508434
Exacrs397508434
Varsomers397508434
Maprs397508434
PheGenIrs397508434
hapmaprs397508434
1000 genomesrs397508434
hgdprs397508434
ensemblrs397508434
gopubmedrs397508434
geneviewrs397508434
scholarrs397508434
googlers397508434
pharmgkbrs397508434
gwascentralrs397508434
openSNPrs397508434
23andMers397508434
23andMe allrs397508434
SNP Nexus

SNPshotrs397508434
SNPdbers397508434
MSV3drs397508434
GWAS Ctlgrs397508434
Max Magnitude0
ClinVar
Risk rs397508434(;)
Alt rs397508434(;)
Reference rs397508434(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117243705delT
CLNSRC ClinVar
CLNACC RCV000046688.2,