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rs387906377

From SNPedia

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


Make rs387906377(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611602
GeneCFTR
is asnp
is mentioned by
dbSNPrs387906377
dbSNP (classic)rs387906377
ClinGenrs387906377
ebirs387906377
HLIrs387906377
Exacrs387906377
Gnomadrs387906377
Varsomers387906377
LitVarrs387906377
Maprs387906377
PheGenIrs387906377
Biobankrs387906377
1000 genomesrs387906377
hgdprs387906377
ensemblrs387906377
geneviewrs387906377
scholarrs387906377
googlers387906377
pharmgkbrs387906377
gwascentralrs387906377
openSNPrs387906377
23andMers387906377
SNPshotrs387906377
SNPdbers387906377
MSV3drs387906377
GWAS Ctlgrs387906377
Max Magnitude3
ClinVar
Risk rs387906377(-;-)
Alt rs387906377(-;-)
Reference Rs387906377(A;A)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251656delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000007642.3,