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rs397508284

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508284(G;T)
Make rs397508284(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117590399
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508284
ebirs397508284
HLIrs397508284
Exacrs397508284
Varsomers397508284
Maprs397508284
PheGenIrs397508284
hapmaprs397508284
1000 genomesrs397508284
hgdprs397508284
ensemblrs397508284
gopubmedrs397508284
geneviewrs397508284
scholarrs397508284
googlers397508284
pharmgkbrs397508284
gwascentralrs397508284
openSNPrs397508284
23andMers397508284
23andMe allrs397508284
SNP Nexus

SNPshotrs397508284
SNPdbers397508284
MSV3drs397508284
GWAS Ctlgrs397508284
Max Magnitude0
ClinVar
Risk rs397508284(T;T)
Alt rs397508284(T;T)
Reference rs397508284(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117230453G>T
CLNSRC ClinVar
CLNACC RCV000046444.2,