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rs74571530

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs74571530(G;G)
Make rs74571530(G;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117559594
GeneCFTR
is asnp
is mentioned by
dbSNPrs74571530
ebirs74571530
HLIrs74571530
Exacrs74571530
Varsomers74571530
Maprs74571530
PheGenIrs74571530
hapmaprs74571530
1000 genomesrs74571530
hgdprs74571530
ensemblrs74571530
gopubmedrs74571530
geneviewrs74571530
scholarrs74571530
googlers74571530
pharmgkbrs74571530
gwascentralrs74571530
openSNPrs74571530
23andMers74571530
23andMe allrs74571530
SNP Nexus

SNPshotrs74571530
SNPdbers74571530
MSV3drs74571530
GWAS Ctlgrs74571530
GMAF0.001837
Max Magnitude0
OMIM602421
Desc
Variant0025
Relatedalso
ClinVar
Risk rs74571530(C,G;C,G)
Alt rs74571530(C,G;C,G)
Reference rs74571530(T;T)
Significance Non-pathogenic
Disease Cystic fibrosis not specified
Variation info
Gene CFTR
CLNDBN Cystic fibrosis not specified
Reversed 0
HGVS NC_000007.13:g.117199648T>C; NC_000007.13:g.117199648T>G
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000046335.2, RCV000007546.3, RCV000078978.4,