Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205658

From SNPedia

Orientationplus
Geno Mag Summary
(CTGGATCCA;CTGGATCCA) 0 common in clinvar
Make rs786205658(-;-)
Make rs786205658(-;CTGGATCCA)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position117548801
GeneCFTR
is asnp
is mentioned by
dbSNPrs786205658
ebirs786205658
HLIrs786205658
Exacrs786205658
Varsomers786205658
Maprs786205658
PheGenIrs786205658
hapmaprs786205658
1000 genomesrs786205658
hgdprs786205658
ensemblrs786205658
gopubmedrs786205658
geneviewrs786205658
scholarrs786205658
googlers786205658
pharmgkbrs786205658
gwascentralrs786205658
openSNPrs786205658
23andMers786205658
23andMe allrs786205658
SNP Nexus

SNPshotrs786205658
SNPdbers786205658
MSV3drs786205658
GWAS Ctlgrs786205658
Max Magnitude0
ClinVar
Risk rs786205658(;)
Alt rs786205658(;)
Reference rs786205658(CTGGATCCA;CTGGATCCA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CFTR
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.117188855_117188863delCTGGATCCA
CLNSRC
CLNACC RCV000171532.1,