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rs797045160

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045160(A;A)
Make rs797045160(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position117542015
GeneCFTR
is asnp
is mentioned by
dbSNPrs797045160
dbSNP (classic)rs797045160
ClinGenrs797045160
ebirs797045160
HLIrs797045160
Exacrs797045160
Gnomadrs797045160
Varsomers797045160
LitVarrs797045160
Maprs797045160
PheGenIrs797045160
Biobankrs797045160
1000 genomesrs797045160
hgdprs797045160
ensemblrs797045160
geneviewrs797045160
scholarrs797045160
googlers797045160
pharmgkbrs797045160
gwascentralrs797045160
openSNPrs797045160
23andMers797045160
SNPshotrs797045160
SNPdbers797045160
MSV3drs797045160
GWAS Ctlgrs797045160
Max Magnitude0
ClinVar
Risk rs797045160(A;A)
Alt rs797045160(A;A)
Reference Rs797045160(G;G)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117182069G>A
CLNSRC CFTR2
CLNACC RCV000191004.1,