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rs397508391

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508391(-;-)
Make rs397508391(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117594947
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508391
ebirs397508391
HLIrs397508391
Exacrs397508391
Varsomers397508391
Maprs397508391
PheGenIrs397508391
hapmaprs397508391
1000 genomesrs397508391
hgdprs397508391
ensemblrs397508391
gopubmedrs397508391
geneviewrs397508391
scholarrs397508391
googlers397508391
pharmgkbrs397508391
gwascentralrs397508391
openSNPrs397508391
23andMers397508391
23andMe allrs397508391
SNP Nexus

SNPshotrs397508391
SNPdbers397508391
MSV3drs397508391
GWAS Ctlgrs397508391
Max Magnitude0
ClinVar
Risk rs397508391(;)
Alt rs397508391(;)
Reference rs397508391(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117235001delT
CLNSRC ClinVar
CLNACC RCV000046611.2,