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rs1800092

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1800092(A;A)
Make rs1800092(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position117559589
GeneCFTR
is asnp
is mentioned by
dbSNPrs1800092
ebirs1800092
HLIrs1800092
Exacrs1800092
Varsomers1800092
Maprs1800092
PheGenIrs1800092
hapmaprs1800092
1000 genomesrs1800092
hgdprs1800092
ensemblrs1800092
gopubmedrs1800092
geneviewrs1800092
scholarrs1800092
googlers1800092
pharmgkbrs1800092
gwascentralrs1800092
openSNPrs1800092
23andMers1800092
23andMe allrs1800092
SNP Nexus

SNPshotrs1800092
SNPdbers1800092
MSV3drs1800092
GWAS Ctlgrs1800092
Max Magnitude0
ClinVar
Risk rs1800092(A,G;A,G)
Alt rs1800092(A,G;A,G)
Reference rs1800092(C;C)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117199643C>G
CLNSRC
CLNACC RCV000046332.2,