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rs1800136

From SNPedia

Orientationplus
Stabilizedplus
Make rs1800136(A;A)
Make rs1800136(A;G)
Make rs1800136(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117667054
GeneCFTR
is asnp
is mentioned by
dbSNPrs1800136
ebirs1800136
HLIrs1800136
Exacrs1800136
Varsomers1800136
Maprs1800136
PheGenIrs1800136
hapmaprs1800136
1000 genomesrs1800136
hgdprs1800136
ensemblrs1800136
gopubmedrs1800136
geneviewrs1800136
scholarrs1800136
googlers1800136
pharmgkbrs1800136
gwascentralrs1800136
openSNPrs1800136
23andMers1800136
23andMe allrs1800136
SNP Nexus

SNPshotrs1800136
SNPdbers1800136
MSV3drs1800136
GWAS Ctlgrs1800136
GMAF0.1781
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19728845] Application of pyrosequencing to the identification of sequence variations in the cystic fibrosis transmembrane conductance regulator gene


[PMID 16436643OA-icon.png] A haplotype framework for cystic fibrosis mutations in Iran.


ClinVar
Risk rs1800136(A;A)
Alt rs1800136(A;A)
Reference rs1800136(G;G)
Significance Other
Disease not specified
Variation info
Gene CFTR
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.117307108G>A
CLNSRC HGMD
CLNACC RCV000079007.7,