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rs397508525

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508525(-;-)
Make rs397508525(-;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611705
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508525
ebirs397508525
HLIrs397508525
Exacrs397508525
Varsomers397508525
Maprs397508525
PheGenIrs397508525
hapmaprs397508525
1000 genomesrs397508525
hgdprs397508525
ensemblrs397508525
gopubmedrs397508525
geneviewrs397508525
scholarrs397508525
googlers397508525
pharmgkbrs397508525
gwascentralrs397508525
openSNPrs397508525
23andMers397508525
23andMe allrs397508525
SNP Nexus

SNPshotrs397508525
SNPdbers397508525
MSV3drs397508525
GWAS Ctlgrs397508525
Max Magnitude0
ClinVar
Risk rs397508525(;)
Alt rs397508525(;)
Reference rs397508525(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251759delC
CLNSRC ClinVar
CLNACC RCV000046841.2,