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rs397508505

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs397508505(-;-)
Make rs397508505(-;GG)
ReferenceGRCh38 38.1/141
Chromosome7
Position117610669
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508505
ebirs397508505
HLIrs397508505
Exacrs397508505
Varsomers397508505
Maprs397508505
PheGenIrs397508505
hapmaprs397508505
1000 genomesrs397508505
hgdprs397508505
ensemblrs397508505
gopubmedrs397508505
geneviewrs397508505
scholarrs397508505
googlers397508505
pharmgkbrs397508505
gwascentralrs397508505
openSNPrs397508505
23andMers397508505
23andMe allrs397508505
SNP Nexus

SNPshotrs397508505
SNPdbers397508505
MSV3drs397508505
GWAS Ctlgrs397508505
Max Magnitude0
ClinVar
Risk rs397508505(;)
Alt rs397508505(;)
Reference rs397508505(GG;GG)
Significance Probable-Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117250723_117250724delGG
CLNSRC ClinVar
CLNACC RCV000046791.3,