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rs746460279

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs746460279(-;-)
Make rs746460279(-;A)
Make rs746460279(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position117592212
GeneCFTR
is asnp
is mentioned by
dbSNPrs746460279
ebirs746460279
HLIrs746460279
Exacrs746460279
Varsomers746460279
Maprs746460279
PheGenIrs746460279
hapmaprs746460279
1000 genomesrs746460279
hgdprs746460279
ensemblrs746460279
gopubmedrs746460279
geneviewrs746460279
scholarrs746460279
googlers746460279
pharmgkbrs746460279
gwascentralrs746460279
openSNPrs746460279
23andMers746460279
23andMe allrs746460279
SNP Nexus

SNPshotrs746460279
SNPdbers746460279
MSV3drs746460279
GWAS Ctlgrs746460279
Max Magnitude0
ClinVar
Risk rs746460279(A;A)
Alt rs746460279(A;A)
Reference rs746460279(;)
Significance Pathogenic
Disease Cystic fibrosis not provided
Variation info
Gene CFTR
CLNDBN Cystic fibrosis not provided
Reversed 0
HGVS NC_000007.13:g.117232273dupA
CLNSRC CFTR2
CLNACC RCV000029493.4, RCV000152995.3,