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rs397508752

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508752(-;-)
Make rs397508752(-;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117534336
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508752
ebirs397508752
HLIrs397508752
Exacrs397508752
Varsomers397508752
Maprs397508752
PheGenIrs397508752
hapmaprs397508752
1000 genomesrs397508752
hgdprs397508752
ensemblrs397508752
gopubmedrs397508752
geneviewrs397508752
scholarrs397508752
googlers397508752
pharmgkbrs397508752
gwascentralrs397508752
openSNPrs397508752
23andMers397508752
23andMe allrs397508752
SNP Nexus

SNPshotrs397508752
SNPdbers397508752
MSV3drs397508752
GWAS Ctlgrs397508752
Max Magnitude0
ClinVar
Risk rs397508752(;)
Alt rs397508752(;)
Reference rs397508752(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117174390delC
CLNSRC ClinVar
CLNACC RCV000047191.2,