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rs377729736

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs377729736(A;G)
Make rs377729736(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531117
GeneCFTR
is asnp
is mentioned by
dbSNPrs377729736
ebirs377729736
HLIrs377729736
Exacrs377729736
Varsomers377729736
Maprs377729736
PheGenIrs377729736
hapmaprs377729736
1000 genomesrs377729736
hgdprs377729736
ensemblrs377729736
gopubmedrs377729736
geneviewrs377729736
scholarrs377729736
googlers377729736
pharmgkbrs377729736
gwascentralrs377729736
openSNPrs377729736
23andMers377729736
23andMe allrs377729736
SNP Nexus

SNPshotrs377729736
SNPdbers377729736
MSV3drs377729736
GWAS Ctlgrs377729736
Max Magnitude0
ClinVar
Risk rs377729736(G;G)
Alt rs377729736(G;G)
Reference rs377729736(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171171A>G
CLNSRC ClinVar
CLNACC RCV000047162.3,