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rs397508482

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508482(-;-)
Make rs397508482(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117610552
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508482
ebirs397508482
HLIrs397508482
Exacrs397508482
Varsomers397508482
Maprs397508482
PheGenIrs397508482
hapmaprs397508482
1000 genomesrs397508482
hgdprs397508482
ensemblrs397508482
gopubmedrs397508482
geneviewrs397508482
scholarrs397508482
googlers397508482
pharmgkbrs397508482
gwascentralrs397508482
openSNPrs397508482
23andMers397508482
23andMe allrs397508482
SNP Nexus

SNPshotrs397508482
SNPdbers397508482
MSV3drs397508482
GWAS Ctlgrs397508482
Max Magnitude0
ClinVar
Risk rs397508482(;)
Alt rs397508482(;)
Reference rs397508482(G;G)
Significance Probable-Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117250606delG
CLNSRC ClinVar
CLNACC RCV000046758.3,