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rs1057517276

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517276(-;A)
Make rs1057517276(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position117592650
GeneCFTR
is asnp
is mentioned by
dbSNPrs1057517276
dbSNP (old)rs1057517276
ClinGenrs1057517276
ebirs1057517276
HLIrs1057517276
Exacrs1057517276
Gnomadrs1057517276
Varsomers1057517276
Maprs1057517276
PheGenIrs1057517276
Biobankrs1057517276
1000 genomesrs1057517276
hgdprs1057517276
ensemblrs1057517276
gopubmedrs1057517276
geneviewrs1057517276
scholarrs1057517276
googlers1057517276
pharmgkbrs1057517276
gwascentralrs1057517276
openSNPrs1057517276
23andMers1057517276
23andMe allrs1057517276
SNPshotrs1057517276
SNPdbers1057517276
MSV3drs1057517276
GWAS Ctlgrs1057517276
Max Magnitude0
ClinVar
Risk rs1057517276(A;A)
Alt rs1057517276(A;A)
Reference Rs1057517276(-;-)
Significance Probable-Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232704dupA
CLNSRC
CLNACC RCV000410112.1,