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rs397508823

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508823(-;-)
Make rs397508823(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540210
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508823
ebirs397508823
HLIrs397508823
Exacrs397508823
Varsomers397508823
Maprs397508823
PheGenIrs397508823
hapmaprs397508823
1000 genomesrs397508823
hgdprs397508823
ensemblrs397508823
gopubmedrs397508823
geneviewrs397508823
scholarrs397508823
googlers397508823
pharmgkbrs397508823
gwascentralrs397508823
openSNPrs397508823
23andMers397508823
23andMe allrs397508823
SNP Nexus

SNPshotrs397508823
SNPdbers397508823
MSV3drs397508823
GWAS Ctlgrs397508823
Max Magnitude0
ClinVar
Risk rs397508823(;)
Alt rs397508823(;)
Reference rs397508823(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180264delT
CLNSRC ClinVar
CLNACC RCV000047302.2,