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rs397508481

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508481(-;-)
Make rs397508481(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117610551
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508481
ebirs397508481
HLIrs397508481
Exacrs397508481
Varsomers397508481
Maprs397508481
PheGenIrs397508481
hapmaprs397508481
1000 genomesrs397508481
hgdprs397508481
ensemblrs397508481
gopubmedrs397508481
geneviewrs397508481
scholarrs397508481
googlers397508481
pharmgkbrs397508481
gwascentralrs397508481
openSNPrs397508481
23andMers397508481
23andMe allrs397508481
SNP Nexus

SNPshotrs397508481
SNPdbers397508481
MSV3drs397508481
GWAS Ctlgrs397508481
Max Magnitude0
ClinVar
Risk rs397508481(;)
Alt rs397508481(;)
Reference rs397508481(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117250605delT
CLNSRC ClinVar
CLNACC RCV000046757.2,