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rs397508390

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508390(-;-)
Make rs397508390(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117594941
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508390
ebirs397508390
HLIrs397508390
Exacrs397508390
Varsomers397508390
Maprs397508390
PheGenIrs397508390
hapmaprs397508390
1000 genomesrs397508390
hgdprs397508390
ensemblrs397508390
gopubmedrs397508390
geneviewrs397508390
scholarrs397508390
googlers397508390
pharmgkbrs397508390
gwascentralrs397508390
openSNPrs397508390
23andMers397508390
23andMe allrs397508390
SNP Nexus

SNPshotrs397508390
SNPdbers397508390
MSV3drs397508390
GWAS Ctlgrs397508390
Max Magnitude0
ClinVar
Risk rs397508390(;)
Alt rs397508390(;)
Reference rs397508390(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117234995delT
CLNSRC ClinVar
CLNACC RCV000046609.2,