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rs397508268

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508268(-;-)
Make rs397508268(-;C)
Make rs397508268(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117590354
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508268
ebirs397508268
HLIrs397508268
Exacrs397508268
Varsomers397508268
Maprs397508268
PheGenIrs397508268
hapmaprs397508268
1000 genomesrs397508268
hgdprs397508268
ensemblrs397508268
gopubmedrs397508268
geneviewrs397508268
scholarrs397508268
googlers397508268
pharmgkbrs397508268
gwascentralrs397508268
openSNPrs397508268
23andMers397508268
23andMe allrs397508268
SNP Nexus

SNPshotrs397508268
SNPdbers397508268
MSV3drs397508268
GWAS Ctlgrs397508268
Max Magnitude0
ClinVar
Risk rs397508268(C;C)
Alt rs397508268(C;C)
Reference rs397508268(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117230409dupC
CLNSRC ClinVar
CLNACC RCV000046419.2,