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

rs397508626

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508626(-;-)
Make rs397508626(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117652844
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508626
ebirs397508626
HLIrs397508626
Exacrs397508626
Varsomers397508626
Maprs397508626
PheGenIrs397508626
hapmaprs397508626
1000 genomesrs397508626
hgdprs397508626
ensemblrs397508626
gopubmedrs397508626
geneviewrs397508626
scholarrs397508626
googlers397508626
pharmgkbrs397508626
gwascentralrs397508626
openSNPrs397508626
23andMers397508626
23andMe allrs397508626
SNP Nexus

SNPshotrs397508626
SNPdbers397508626
MSV3drs397508626
GWAS Ctlgrs397508626
Max Magnitude0
ClinVar
Risk rs397508626(;)
Alt rs397508626(;)
Reference rs397508626(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117292898delA
CLNSRC ClinVar
CLNACC RCV000047012.2,