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rs397508627

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508627(-;-)
Make rs397508627(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531012
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508627
ebirs397508627
HLIrs397508627
Exacrs397508627
Varsomers397508627
Maprs397508627
PheGenIrs397508627
hapmaprs397508627
1000 genomesrs397508627
hgdprs397508627
ensemblrs397508627
gopubmedrs397508627
geneviewrs397508627
scholarrs397508627
googlers397508627
pharmgkbrs397508627
gwascentralrs397508627
openSNPrs397508627
23andMers397508627
23andMe allrs397508627
SNP Nexus

SNPshotrs397508627
SNPdbers397508627
MSV3drs397508627
GWAS Ctlgrs397508627
Max Magnitude0
ClinVar
Risk rs397508627(;)
Alt rs397508627(;)
Reference rs397508627(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171066delT
CLNSRC ClinVar
CLNACC RCV000047013.2,