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rs397508561

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508561(A;A)
Make rs397508561(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117614680
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508561
ebirs397508561
HLIrs397508561
Exacrs397508561
Varsomers397508561
Maprs397508561
PheGenIrs397508561
hapmaprs397508561
1000 genomesrs397508561
hgdprs397508561
ensemblrs397508561
gopubmedrs397508561
geneviewrs397508561
scholarrs397508561
googlers397508561
pharmgkbrs397508561
gwascentralrs397508561
openSNPrs397508561
23andMers397508561
23andMe allrs397508561
SNP Nexus

SNPshotrs397508561
SNPdbers397508561
MSV3drs397508561
GWAS Ctlgrs397508561
Max Magnitude0
ClinVar
Risk rs397508561(A;A)
Alt rs397508561(A;A)
Reference rs397508561(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117254734G>A
CLNSRC ClinVar
CLNACC RCV000046889.2,