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

rs397508148

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508148(C;T)
Make rs397508148(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540287
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508148
ebirs397508148
HLIrs397508148
Exacrs397508148
Varsomers397508148
Maprs397508148
PheGenIrs397508148
hapmaprs397508148
1000 genomesrs397508148
hgdprs397508148
ensemblrs397508148
gopubmedrs397508148
geneviewrs397508148
scholarrs397508148
googlers397508148
pharmgkbrs397508148
gwascentralrs397508148
openSNPrs397508148
23andMers397508148
23andMe allrs397508148
SNP Nexus

SNPshotrs397508148
SNPdbers397508148
MSV3drs397508148
GWAS Ctlgrs397508148
Max Magnitude0
ClinVar
Risk rs397508148(T;T)
Alt rs397508148(T;T)
Reference rs397508148(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180341C>T
CLNSRC ClinVar
CLNACC RCV000046215.2,