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rs397508783

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508783(A;A)
Make rs397508783(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117535363
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508783
ebirs397508783
HLIrs397508783
Exacrs397508783
Varsomers397508783
Maprs397508783
PheGenIrs397508783
hapmaprs397508783
1000 genomesrs397508783
hgdprs397508783
ensemblrs397508783
gopubmedrs397508783
geneviewrs397508783
scholarrs397508783
googlers397508783
pharmgkbrs397508783
gwascentralrs397508783
openSNPrs397508783
23andMers397508783
23andMe allrs397508783
SNP Nexus

SNPshotrs397508783
SNPdbers397508783
MSV3drs397508783
GWAS Ctlgrs397508783
Max Magnitude0
ClinVar
Risk rs397508783(A;A)
Alt rs397508783(A;A)
Reference rs397508783(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117175417T>A
CLNSRC ClinVar
CLNACC RCV000047235.2,