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rs397508250

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508250(A;G)
Make rs397508250(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117509032
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508250
ebirs397508250
HLIrs397508250
Exacrs397508250
Varsomers397508250
Maprs397508250
PheGenIrs397508250
hapmaprs397508250
1000 genomesrs397508250
hgdprs397508250
ensemblrs397508250
gopubmedrs397508250
geneviewrs397508250
scholarrs397508250
googlers397508250
pharmgkbrs397508250
gwascentralrs397508250
openSNPrs397508250
23andMers397508250
23andMe allrs397508250
SNP Nexus

SNPshotrs397508250
SNPdbers397508250
MSV3drs397508250
GWAS Ctlgrs397508250
Max Magnitude0
ClinVar
Risk rs397508250(G;G)
Alt rs397508250(G;G)
Reference rs397508250(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117149086A>G
CLNSRC ClinVar
CLNACC RCV000046383.2,