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rs397508424

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508424(-;-)
Make rs397508424(-;G)
Make rs397508424(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117603610
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508424
ebirs397508424
HLIrs397508424
Exacrs397508424
Varsomers397508424
Maprs397508424
PheGenIrs397508424
hapmaprs397508424
1000 genomesrs397508424
hgdprs397508424
ensemblrs397508424
gopubmedrs397508424
geneviewrs397508424
scholarrs397508424
googlers397508424
pharmgkbrs397508424
gwascentralrs397508424
openSNPrs397508424
23andMers397508424
23andMe allrs397508424
SNP Nexus

SNPshotrs397508424
SNPdbers397508424
MSV3drs397508424
GWAS Ctlgrs397508424
Max Magnitude0
ClinVar
Risk rs397508424(G;G)
Alt rs397508424(G;G)
Reference rs397508424(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117243664dupG
CLNSRC ClinVar
CLNACC RCV000046667.2,