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rs387906373

From SNPedia

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


Make rs387906373(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117652846
GeneCFTR
is asnp
is mentioned by
dbSNPrs387906373
dbSNP (classic)rs387906373
ClinGenrs387906373
ebirs387906373
HLIrs387906373
Exacrs387906373
Gnomadrs387906373
Varsomers387906373
LitVarrs387906373
Maprs387906373
PheGenIrs387906373
Biobankrs387906373
1000 genomesrs387906373
hgdprs387906373
ensemblrs387906373
geneviewrs387906373
scholarrs387906373
googlers387906373
pharmgkbrs387906373
gwascentralrs387906373
openSNPrs387906373
23andMers387906373
SNPshotrs387906373
SNPdbers387906373
MSV3drs387906373
GWAS Ctlgrs387906373
Merged fromRs397508628, Rs397508629
Max Magnitude3
ClinVar
Risk rs387906373(-;-) rs387906373(ATTT;ATTT)
Alt rs387906373(-;-) rs387906373(ATTT;ATTT)
Reference Rs387906373(TATT;TATT)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117292905_117292908delATTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000047015.6,