Have questions? Visit https://www.reddit.com/r/SNPedia

rs1800091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1800091(A;G)
Make rs1800091(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117559587
GeneCFTR
is asnp
is mentioned by
dbSNPrs1800091
ebirs1800091
HLIrs1800091
Exacrs1800091
Varsomers1800091
Maprs1800091
PheGenIrs1800091
hapmaprs1800091
1000 genomesrs1800091
hgdprs1800091
ensemblrs1800091
gopubmedrs1800091
geneviewrs1800091
scholarrs1800091
googlers1800091
pharmgkbrs1800091
gwascentralrs1800091
openSNPrs1800091
23andMers1800091
23andMe allrs1800091
SNP Nexus

SNPshotrs1800091
SNPdbers1800091
MSV3drs1800091
GWAS Ctlgrs1800091
Max Magnitude0
OMIM602421
Desc
Variant0024
Relatedalso
ClinVar
Risk rs1800091(C,G;C,G)
Alt rs1800091(C,G;C,G)
Reference rs1800091(A;A)
Significance Non-pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117199641A>C; NC_000007.13:g.117199641A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000046329.2, RCV000007551.3,