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rs150914702

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150914702(A;A)
Make rs150914702(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117667110
GeneCFTR
is asnp
is mentioned by
dbSNPrs150914702
ebirs150914702
HLIrs150914702
Exacrs150914702
Varsomers150914702
Maprs150914702
PheGenIrs150914702
hapmaprs150914702
1000 genomesrs150914702
hgdprs150914702
ensemblrs150914702
gopubmedrs150914702
geneviewrs150914702
scholarrs150914702
googlers150914702
pharmgkbrs150914702
gwascentralrs150914702
openSNPrs150914702
23andMers150914702
23andMe allrs150914702
SNP Nexus

SNPshotrs150914702
SNPdbers150914702
MSV3drs150914702
GWAS Ctlgrs150914702
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs150914702(A;A)
Alt rs150914702(A;A)
Reference rs150914702(G;G)
Significance Untested
Disease Cystic fibrosis not provided
Variation info
Gene CFTR
CLNDBN Cystic fibrosis not provided
Reversed 0
HGVS NC_000007.13:g.117307164G>A
CLNSRC ClinVar
CLNACC RCV000046187.2, RCV000176720.1,