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rs397508534

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508534(-;-)
Make rs397508534(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611735
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508534
ClinGenrs397508534
ebirs397508534
HLIrs397508534
Exacrs397508534
Varsomers397508534
Maprs397508534
PheGenIrs397508534
hapmaprs397508534
1000 genomesrs397508534
hgdprs397508534
ensemblrs397508534
gopubmedrs397508534
geneviewrs397508534
scholarrs397508534
googlers397508534
pharmgkbrs397508534
gwascentralrs397508534
openSNPrs397508534
23andMers397508534
23andMe allrs397508534
SNP Nexus

SNPshotrs397508534
SNPdbers397508534
MSV3drs397508534
GWAS Ctlgrs397508534
Max Magnitude0
ClinVar
Risk rs397508534(-;-)
Alt rs397508534(-;-)
Reference Rs397508534(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251789delG
CLNSRC ClinVar
CLNACC RCV000046857.2,