Have questions? Visit https://www.reddit.com/r/SNPedia

rs397508150

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508150(A;A)
Make rs397508150(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540298
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508150
ebirs397508150
HLIrs397508150
Exacrs397508150
Varsomers397508150
Maprs397508150
PheGenIrs397508150
hapmaprs397508150
1000 genomesrs397508150
hgdprs397508150
ensemblrs397508150
gopubmedrs397508150
geneviewrs397508150
scholarrs397508150
googlers397508150
pharmgkbrs397508150
gwascentralrs397508150
openSNPrs397508150
23andMers397508150
23andMe allrs397508150
SNP Nexus

SNPshotrs397508150
SNPdbers397508150
MSV3drs397508150
GWAS Ctlgrs397508150
Max Magnitude0
ClinVar
Risk rs397508150(A;A)
Alt rs397508150(A;A)
Reference rs397508150(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180352G>A
CLNSRC ClinVar
CLNACC RCV000046218.2,