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rs121908809

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908809(-;-)
Make rs121908809(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592143
GeneCFTR
is asnp
is mentioned by
dbSNPrs121908809
ebirs121908809
HLIrs121908809
Exacrs121908809
Varsomers121908809
Maprs121908809
PheGenIrs121908809
hapmaprs121908809
1000 genomesrs121908809
hgdprs121908809
ensemblrs121908809
gopubmedrs121908809
geneviewrs121908809
scholarrs121908809
googlers121908809
pharmgkbrs121908809
gwascentralrs121908809
openSNPrs121908809
23andMers121908809
23andMe allrs121908809
SNP Nexus

SNPshotrs121908809
SNPdbers121908809
MSV3drs121908809
GWAS Ctlgrs121908809
Max Magnitude0
ClinVar
Risk rs121908809(;)
Alt rs121908809(;)
Reference rs121908809(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232197delA
CLNSRC ClinVar
CLNACC RCV000046512.2,