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rs397508270

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508270(A;G)
Make rs397508270(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117590367
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508270
ebirs397508270
HLIrs397508270
Exacrs397508270
Varsomers397508270
Maprs397508270
PheGenIrs397508270
hapmaprs397508270
1000 genomesrs397508270
hgdprs397508270
ensemblrs397508270
gopubmedrs397508270
geneviewrs397508270
scholarrs397508270
googlers397508270
pharmgkbrs397508270
gwascentralrs397508270
openSNPrs397508270
23andMers397508270
23andMe allrs397508270
SNP Nexus

SNPshotrs397508270
SNPdbers397508270
MSV3drs397508270
GWAS Ctlgrs397508270
Max Magnitude0
ClinVar
Risk rs397508270(G;G)
Alt rs397508270(G;G)
Reference rs397508270(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117230421A>G
CLNSRC ClinVar
CLNACC RCV000046426.2,