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rs397508258

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508258(-;-)
Make rs397508258(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117587828
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508258
ebirs397508258
HLIrs397508258
Exacrs397508258
Varsomers397508258
Maprs397508258
PheGenIrs397508258
hapmaprs397508258
1000 genomesrs397508258
hgdprs397508258
ensemblrs397508258
gopubmedrs397508258
geneviewrs397508258
scholarrs397508258
googlers397508258
pharmgkbrs397508258
gwascentralrs397508258
openSNPrs397508258
23andMers397508258
23andMe allrs397508258
SNP Nexus

SNPshotrs397508258
SNPdbers397508258
MSV3drs397508258
GWAS Ctlgrs397508258
Max Magnitude0
ClinVar
Risk rs397508258(;)
Alt rs397508258(;)
Reference rs397508258(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117227882delA
CLNSRC ClinVar
CLNACC RCV000046402.2,