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

rs397508261

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508261(G;T)
Make rs397508261(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117589476
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508261
ebirs397508261
HLIrs397508261
Exacrs397508261
Varsomers397508261
Maprs397508261
PheGenIrs397508261
hapmaprs397508261
1000 genomesrs397508261
hgdprs397508261
ensemblrs397508261
gopubmedrs397508261
geneviewrs397508261
scholarrs397508261
googlers397508261
pharmgkbrs397508261
gwascentralrs397508261
openSNPrs397508261
23andMers397508261
23andMe allrs397508261
SNP Nexus

SNPshotrs397508261
SNPdbers397508261
MSV3drs397508261
GWAS Ctlgrs397508261
Max Magnitude0
ClinVar
Risk rs397508261(T;T)
Alt rs397508261(T;T)
Reference rs397508261(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117229530G>T
CLNSRC ClinVar
CLNACC RCV000046407.2,