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rs1057517032

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517032(-;-)
Make rs1057517032(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position117603728
GeneCFTR
is asnp
is mentioned by
dbSNPrs1057517032
dbSNP (old)rs1057517032
ClinGenrs1057517032
ebirs1057517032
HLIrs1057517032
Exacrs1057517032
Gnomadrs1057517032
Varsomers1057517032
Maprs1057517032
PheGenIrs1057517032
Biobankrs1057517032
1000 genomesrs1057517032
hgdprs1057517032
ensemblrs1057517032
gopubmedrs1057517032
geneviewrs1057517032
scholarrs1057517032
googlers1057517032
pharmgkbrs1057517032
gwascentralrs1057517032
openSNPrs1057517032
23andMers1057517032
23andMe allrs1057517032
SNPshotrs1057517032
SNPdbers1057517032
MSV3drs1057517032
GWAS Ctlgrs1057517032
Max Magnitude0
ClinVar
Risk rs1057517032(-;-)
Alt rs1057517032(-;-)
Reference Rs1057517032(A;A)
Significance Probable-Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117243782delA
CLNSRC
CLNACC RCV000409306.1,