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rs397508518

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs397508518(-;-)
Make rs397508518(-;CT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611670
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508518
ebirs397508518
HLIrs397508518
Exacrs397508518
Varsomers397508518
Maprs397508518
PheGenIrs397508518
hapmaprs397508518
1000 genomesrs397508518
hgdprs397508518
ensemblrs397508518
gopubmedrs397508518
geneviewrs397508518
scholarrs397508518
googlers397508518
pharmgkbrs397508518
gwascentralrs397508518
openSNPrs397508518
23andMers397508518
23andMe allrs397508518
SNP Nexus

SNPshotrs397508518
SNPdbers397508518
MSV3drs397508518
GWAS Ctlgrs397508518
Max Magnitude0
ClinVar
Risk rs397508518(;)
Alt rs397508518(;)
Reference rs397508518(CT;CT)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251724_117251725delCT
CLNSRC ClinVar
CLNACC RCV000046830.2,