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rs387906368

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906368(A;A)
Make rs387906368(A;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position117587755
GeneCFTR
is asnp
is mentioned by
dbSNPrs387906368
ebirs387906368
HLIrs387906368
Exacrs387906368
Varsomers387906368
Maprs387906368
PheGenIrs387906368
hapmaprs387906368
1000 genomesrs387906368
hgdprs387906368
ensemblrs387906368
gopubmedrs387906368
geneviewrs387906368
scholarrs387906368
googlers387906368
pharmgkbrs387906368
gwascentralrs387906368
openSNPrs387906368
23andMers387906368
23andMe allrs387906368
SNP Nexus

SNPshotrs387906368
SNPdbers387906368
MSV3drs387906368
GWAS Ctlgrs387906368
Max Magnitude0
ClinVar
Risk rs387906368(A;A)
Alt rs387906368(A;A)
Reference rs387906368(C;C)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117227809C>A
CLNSRC Cystic Fibrosis Mutation Database OMIM Allelic Variant
CLNACC RCV000007593.3,