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rs397508726

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508726(-;-)
Make rs397508726(-;T)
Make rs397508726(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531098
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508726
ebirs397508726
HLIrs397508726
Exacrs397508726
Varsomers397508726
Maprs397508726
PheGenIrs397508726
hapmaprs397508726
1000 genomesrs397508726
hgdprs397508726
ensemblrs397508726
gopubmedrs397508726
geneviewrs397508726
scholarrs397508726
googlers397508726
pharmgkbrs397508726
gwascentralrs397508726
openSNPrs397508726
23andMers397508726
23andMe allrs397508726
SNP Nexus

SNPshotrs397508726
SNPdbers397508726
MSV3drs397508726
GWAS Ctlgrs397508726
Max Magnitude0
ClinVar
Risk rs397508726(T;T)
Alt rs397508726(T;T)
Reference rs397508726(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171153dupT
CLNSRC ClinVar
CLNACC RCV000047150.2,