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rs1057516646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057516646(A;G)
Make rs1057516646(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position117536546
GeneCFTR
is asnp
is mentioned by
dbSNPrs1057516646
dbSNP (old)rs1057516646
ClinGenrs1057516646
ebirs1057516646
HLIrs1057516646
Exacrs1057516646
Gnomadrs1057516646
Varsomers1057516646
Maprs1057516646
PheGenIrs1057516646
Biobankrs1057516646
1000 genomesrs1057516646
hgdprs1057516646
ensemblrs1057516646
gopubmedrs1057516646
geneviewrs1057516646
scholarrs1057516646
googlers1057516646
pharmgkbrs1057516646
gwascentralrs1057516646
openSNPrs1057516646
23andMers1057516646
23andMe allrs1057516646
SNPshotrs1057516646
SNPdbers1057516646
MSV3drs1057516646
GWAS Ctlgrs1057516646
Max Magnitude0
ClinVar
Risk rs1057516646(G;G)
Alt rs1057516646(G;G)
Reference Rs1057516646(A;A)
Significance Probable-Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117176600A>G
CLNSRC
CLNACC RCV000411056.1,