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rs397508406

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508406(-;-)
Make rs397508406(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117595041
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508406
ebirs397508406
HLIrs397508406
Exacrs397508406
Varsomers397508406
Maprs397508406
PheGenIrs397508406
hapmaprs397508406
1000 genomesrs397508406
hgdprs397508406
ensemblrs397508406
gopubmedrs397508406
geneviewrs397508406
scholarrs397508406
googlers397508406
pharmgkbrs397508406
gwascentralrs397508406
openSNPrs397508406
23andMers397508406
23andMe allrs397508406
SNP Nexus

SNPshotrs397508406
SNPdbers397508406
MSV3drs397508406
GWAS Ctlgrs397508406
Max Magnitude0
ClinVar
Risk rs397508406(;)
Alt rs397508406(;)
Reference rs397508406(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117235095delG
CLNSRC ClinVar
CLNACC RCV000046632.2,