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rs397508351

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508351(-;-)
Make rs397508351(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592370
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508351
ebirs397508351
HLIrs397508351
Exacrs397508351
Varsomers397508351
Maprs397508351
PheGenIrs397508351
hapmaprs397508351
1000 genomesrs397508351
hgdprs397508351
ensemblrs397508351
gopubmedrs397508351
geneviewrs397508351
scholarrs397508351
googlers397508351
pharmgkbrs397508351
gwascentralrs397508351
openSNPrs397508351
23andMers397508351
23andMe allrs397508351
SNP Nexus

SNPshotrs397508351
SNPdbers397508351
MSV3drs397508351
GWAS Ctlgrs397508351
Max Magnitude0
ClinVar
Risk rs397508351(;)
Alt rs397508351(;)
Reference rs397508351(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232424delA
CLNSRC ClinVar
CLNACC RCV000046552.2,