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rs1800082

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1800082(C;G)
Make rs1800082(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117535409
GeneCFTR
is asnp
is mentioned by
dbSNPrs1800082
ebirs1800082
HLIrs1800082
Exacrs1800082
Varsomers1800082
Maprs1800082
PheGenIrs1800082
hapmaprs1800082
1000 genomesrs1800082
hgdprs1800082
ensemblrs1800082
gopubmedrs1800082
geneviewrs1800082
scholarrs1800082
googlers1800082
pharmgkbrs1800082
gwascentralrs1800082
openSNPrs1800082
23andMers1800082
23andMe allrs1800082
SNP Nexus

SNPshotrs1800082
SNPdbers1800082
MSV3drs1800082
GWAS Ctlgrs1800082
Max Magnitude0
ClinVar
Risk rs1800082(G,T;G,T)
Alt rs1800082(G,T;G,T)
Reference rs1800082(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117175463C>G
CLNSRC ClinVar
CLNACC RCV000047245.2,