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rs143570767

From SNPedia

Cystic Fibrosis related
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 3 cystic fibrosis carrier
(G;G) 0 common in clinvar


Make rs143570767(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117642594
GeneCFTR
is asnp
is mentioned by
dbSNPrs143570767
ebirs143570767
HLIrs143570767
Exacrs143570767
Varsomers143570767
Maprs143570767
PheGenIrs143570767
hapmaprs143570767
1000 genomesrs143570767
hgdprs143570767
ensemblrs143570767
gopubmedrs143570767
geneviewrs143570767
scholarrs143570767
googlers143570767
pharmgkbrs143570767
gwascentralrs143570767
openSNPrs143570767
23andMers143570767
23andMe allrs143570767
SNP Nexus

SNPshotrs143570767
SNPdbers143570767
MSV3drs143570767
GWAS Ctlgrs143570767
Max Magnitude3

Cystic fibrosis; c.3873+1G>A


ClinVar
Risk rs143570767(A;A)
Alt rs143570767(A;A)
Reference rs143570767(G;G)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117282648G>A
CLNSRC CFTR2 OMIM Allelic Variant
CLNACC RCV000007580.5,