Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057516970

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516970(-;-)
Make rs1057516970(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position117627548
GeneCFTR
is asnp
is mentioned by
dbSNPrs1057516970
dbSNP (old)rs1057516970
ClinGenrs1057516970
ebirs1057516970
HLIrs1057516970
Exacrs1057516970
Gnomadrs1057516970
Varsomers1057516970
Maprs1057516970
PheGenIrs1057516970
Biobankrs1057516970
1000 genomesrs1057516970
hgdprs1057516970
ensemblrs1057516970
gopubmedrs1057516970
geneviewrs1057516970
scholarrs1057516970
googlers1057516970
pharmgkbrs1057516970
gwascentralrs1057516970
openSNPrs1057516970
23andMers1057516970
23andMe allrs1057516970
SNPshotrs1057516970
SNPdbers1057516970
MSV3drs1057516970
GWAS Ctlgrs1057516970
Max Magnitude0
ClinVar
Risk rs1057516970(-;-)
Alt rs1057516970(-;-)
Reference Rs1057516970(G;G)
Significance Probable-Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267602delG
CLNSRC
CLNACC RCV000410780.1,