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rs387906364

From SNPedia

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


Make rs387906364(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531054
GeneCFTR
is asnp
is mentioned by
dbSNPrs387906364
ebirs387906364
HLIrs387906364
Exacrs387906364
Varsomers387906364
Maprs387906364
PheGenIrs387906364
hapmaprs387906364
1000 genomesrs387906364
hgdprs387906364
ensemblrs387906364
gopubmedrs387906364
geneviewrs387906364
scholarrs387906364
googlers387906364
pharmgkbrs387906364
gwascentralrs387906364
openSNPrs387906364
23andMers387906364
23andMe allrs387906364
SNP Nexus

SNPshotrs387906364
SNPdbers387906364
MSV3drs387906364
GWAS Ctlgrs387906364
Max Magnitude3
ClinVar
Risk rs387906364(;)
Alt rs387906364(;)
Reference rs387906364(T;T)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171108delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000007567.3,