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rs1060503164

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503164(A;A)
Make rs1060503164(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position117603783
GeneCFTR
is asnp
is mentioned by
dbSNPrs1060503164
dbSNP (old)rs1060503164
ClinGenrs1060503164
ebirs1060503164
HLIrs1060503164
Exacrs1060503164
Gnomadrs1060503164
Varsomers1060503164
Maprs1060503164
PheGenIrs1060503164
Biobankrs1060503164
1000 genomesrs1060503164
hgdprs1060503164
ensemblrs1060503164
gopubmedrs1060503164
geneviewrs1060503164
scholarrs1060503164
googlers1060503164
pharmgkbrs1060503164
gwascentralrs1060503164
openSNPrs1060503164
23andMers1060503164
23andMe allrs1060503164
SNPshotrs1060503164
SNPdbers1060503164
MSV3drs1060503164
GWAS Ctlgrs1060503164
Max Magnitude0
ClinVar
Risk rs1060503164(A;A)
Alt rs1060503164(A;A)
Reference Rs1060503164(G;G)
Significance Probable-Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117243837G>A
CLNSRC
CLNACC RCV000465662.1,