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rs397508497

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508497(-;-)
Make rs397508497(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117610636
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508497
ebirs397508497
HLIrs397508497
Exacrs397508497
Varsomers397508497
Maprs397508497
PheGenIrs397508497
hapmaprs397508497
1000 genomesrs397508497
hgdprs397508497
ensemblrs397508497
gopubmedrs397508497
geneviewrs397508497
scholarrs397508497
googlers397508497
pharmgkbrs397508497
gwascentralrs397508497
openSNPrs397508497
23andMers397508497
23andMe allrs397508497
SNP Nexus

SNPshotrs397508497
SNPdbers397508497
MSV3drs397508497
GWAS Ctlgrs397508497
Max Magnitude0
ClinVar
Risk rs397508497(;)
Alt rs397508497(;)
Reference rs397508497(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117250690delA
CLNSRC ClinVar
CLNACC RCV000046782.2,