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rs35396083

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs35396083(-;-)
Make rs35396083(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627676
GeneCFTR
is asnp
is mentioned by
dbSNPrs35396083
ebirs35396083
HLIrs35396083
Exacrs35396083
Varsomers35396083
Maprs35396083
PheGenIrs35396083
hapmaprs35396083
1000 genomesrs35396083
hgdprs35396083
ensemblrs35396083
gopubmedrs35396083
geneviewrs35396083
scholarrs35396083
googlers35396083
pharmgkbrs35396083
gwascentralrs35396083
openSNPrs35396083
23andMers35396083
23andMe allrs35396083
SNP Nexus

SNPshotrs35396083
SNPdbers35396083
MSV3drs35396083
GWAS Ctlgrs35396083
Max Magnitude0
ClinVar
Risk rs35396083(;)
Alt rs35396083(;)
Reference rs35396083(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267730delG
CLNSRC ClinVar
CLNACC RCV000046940.2,