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

rs148173473

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs148173473(A;G)
Make rs148173473(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117587760
GeneCFTR
is asnp
is mentioned by
dbSNPrs148173473
ebirs148173473
HLIrs148173473
Exacrs148173473
Varsomers148173473
Maprs148173473
PheGenIrs148173473
hapmaprs148173473
1000 genomesrs148173473
hgdprs148173473
ensemblrs148173473
gopubmedrs148173473
geneviewrs148173473
scholarrs148173473
googlers148173473
pharmgkbrs148173473
gwascentralrs148173473
openSNPrs148173473
23andMers148173473
23andMe allrs148173473
SNP Nexus

SNPshotrs148173473
SNPdbers148173473
MSV3drs148173473
GWAS Ctlgrs148173473
Max Magnitude0
ClinVar
Risk rs148173473(G,T;G,T)
Alt rs148173473(G,T;G,T)
Reference rs148173473(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117227814A>T
CLNSRC ClinVar
CLNACC RCV000046360.2,