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rs397508650

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508650(A;A)
Make rs397508650(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117652933
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508650
ebirs397508650
HLIrs397508650
Exacrs397508650
Varsomers397508650
Maprs397508650
PheGenIrs397508650
hapmaprs397508650
1000 genomesrs397508650
hgdprs397508650
ensemblrs397508650
gopubmedrs397508650
geneviewrs397508650
scholarrs397508650
googlers397508650
pharmgkbrs397508650
gwascentralrs397508650
openSNPrs397508650
23andMers397508650
23andMe allrs397508650
SNP Nexus

SNPshotrs397508650
SNPdbers397508650
MSV3drs397508650
GWAS Ctlgrs397508650
Max Magnitude0
ClinVar
Risk rs397508650(A;A)
Alt rs397508650(A;A)
Reference rs397508650(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117292987T>A
CLNSRC ClinVar
CLNACC RCV000047045.2,