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rs79635528

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 3 cystic fibrosis carrier
Make rs79635528(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611695
GeneCFTR
is asnp
is mentioned by
dbSNPrs79635528
ebirs79635528
HLIrs79635528
Exacrs79635528
Varsomers79635528
Maprs79635528
PheGenIrs79635528
hapmaprs79635528
1000 genomesrs79635528
hgdprs79635528
ensemblrs79635528
gopubmedrs79635528
geneviewrs79635528
scholarrs79635528
googlers79635528
pharmgkbrs79635528
gwascentralrs79635528
openSNPrs79635528
23andMers79635528
23andMe allrs79635528
SNP Nexus

SNPshotrs79635528
SNPdbers79635528
MSV3drs79635528
GWAS Ctlgrs79635528
Max Magnitude3
OMIM602421
Desc
Variant0105
Relatedalso
ClinVar
Risk rs79635528(G;G)
Alt rs79635528(G;G)
Reference rs79635528(A;A)
Significance Other
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251749A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007631.5,