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rs397508737

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508737(-;-)
Make rs397508737(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117534280
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508737
ebirs397508737
HLIrs397508737
Exacrs397508737
Varsomers397508737
Maprs397508737
PheGenIrs397508737
hapmaprs397508737
1000 genomesrs397508737
hgdprs397508737
ensemblrs397508737
gopubmedrs397508737
geneviewrs397508737
scholarrs397508737
googlers397508737
pharmgkbrs397508737
gwascentralrs397508737
openSNPrs397508737
23andMers397508737
23andMe allrs397508737
SNP Nexus

SNPshotrs397508737
SNPdbers397508737
MSV3drs397508737
GWAS Ctlgrs397508737
Max Magnitude0
ClinVar
Risk rs397508737(;)
Alt rs397508737(;)
Reference rs397508737(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117174334delT
CLNSRC ClinVar
CLNACC RCV000047168.2,