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rs397508716

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508716(G;T)
Make rs397508716(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117667082
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508716
ebirs397508716
HLIrs397508716
Exacrs397508716
Varsomers397508716
Maprs397508716
PheGenIrs397508716
hapmaprs397508716
1000 genomesrs397508716
hgdprs397508716
ensemblrs397508716
gopubmedrs397508716
geneviewrs397508716
scholarrs397508716
googlers397508716
pharmgkbrs397508716
gwascentralrs397508716
openSNPrs397508716
23andMers397508716
23andMe allrs397508716
SNP Nexus

SNPshotrs397508716
SNPdbers397508716
MSV3drs397508716
GWAS Ctlgrs397508716
Max Magnitude0
ClinVar
Risk rs397508716(T;T)
Alt rs397508716(T;T)
Reference rs397508716(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117307136G>T
CLNSRC ClinVar
CLNACC RCV000047134.2,