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rs397508707

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508707(G;T)
Make rs397508707(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117666917
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508707
ebirs397508707
HLIrs397508707
Exacrs397508707
Varsomers397508707
Maprs397508707
PheGenIrs397508707
hapmaprs397508707
1000 genomesrs397508707
hgdprs397508707
ensemblrs397508707
gopubmedrs397508707
geneviewrs397508707
scholarrs397508707
googlers397508707
pharmgkbrs397508707
gwascentralrs397508707
openSNPrs397508707
23andMers397508707
23andMe allrs397508707
SNP Nexus

SNPshotrs397508707
SNPdbers397508707
MSV3drs397508707
GWAS Ctlgrs397508707
Max Magnitude0
ClinVar
Risk rs397508707(T;T)
Alt rs397508707(T;T)
Reference rs397508707(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117306971G>T
CLNSRC ClinVar
CLNACC RCV000047120.2,