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rs387906363

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;A) 3 cystic fibrosis carrier
(A;A) 0 common in clinvar


Make rs387906363(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531049
GeneCFTR
is asnp
is mentioned by
dbSNPrs387906363
ebirs387906363
HLIrs387906363
Exacrs387906363
Varsomers387906363
Maprs387906363
PheGenIrs387906363
hapmaprs387906363
1000 genomesrs387906363
hgdprs387906363
ensemblrs387906363
gopubmedrs387906363
geneviewrs387906363
scholarrs387906363
googlers387906363
pharmgkbrs387906363
gwascentralrs387906363
openSNPrs387906363
23andMers387906363
23andMe allrs387906363
SNP Nexus

SNPshotrs387906363
SNPdbers387906363
MSV3drs387906363
GWAS Ctlgrs387906363
Max Magnitude3
ClinVar
Risk rs387906363(;)
Alt rs387906363(;)
Reference rs387906363(A;A)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171103delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000007566.3,