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rs1057516236

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516236(-;-)
Make rs1057516236(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position117592596
GeneCFTR
is asnp
is mentioned by
dbSNPrs1057516236
dbSNP (old)rs1057516236
ClinGenrs1057516236
ebirs1057516236
HLIrs1057516236
Exacrs1057516236
Gnomadrs1057516236
Varsomers1057516236
LitVarrs1057516236
Maprs1057516236
PheGenIrs1057516236
Biobankrs1057516236
1000 genomesrs1057516236
hgdprs1057516236
ensemblrs1057516236
gopubmedrs1057516236
geneviewrs1057516236
scholarrs1057516236
googlers1057516236
pharmgkbrs1057516236
gwascentralrs1057516236
openSNPrs1057516236
23andMers1057516236
23andMe allrs1057516236
SNPshotrs1057516236
SNPdbers1057516236
MSV3drs1057516236
GWAS Ctlgrs1057516236
Max Magnitude0
ClinVar
Risk rs1057516236(-;-)
Alt rs1057516236(-;-)
Reference Rs1057516236(G;G)
Significance Probable-Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232650delG
CLNSRC
CLNACC RCV000410071.1,