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rs397508714

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508714(-;-)
Make rs397508714(-;T)
Make rs397508714(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117480137
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508714
ebirs397508714
HLIrs397508714
Exacrs397508714
Varsomers397508714
Maprs397508714
PheGenIrs397508714
hapmaprs397508714
1000 genomesrs397508714
hgdprs397508714
ensemblrs397508714
gopubmedrs397508714
geneviewrs397508714
scholarrs397508714
googlers397508714
pharmgkbrs397508714
gwascentralrs397508714
openSNPrs397508714
23andMers397508714
23andMe allrs397508714
SNP Nexus

SNPshotrs397508714
SNPdbers397508714
MSV3drs397508714
GWAS Ctlgrs397508714
Max Magnitude0
ClinVar
Risk rs397508714(T;T)
Alt rs397508714(T;T)
Reference rs397508714(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117120192dupT
CLNSRC ClinVar
CLNACC RCV000047132.2,