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rs786204693

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204693(-;-)
Make rs786204693(-;A)
Make rs786204693(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position117536654
GeneCFTR
is asnp
is mentioned by
dbSNPrs786204693
ebirs786204693
HLIrs786204693
Exacrs786204693
Varsomers786204693
Maprs786204693
PheGenIrs786204693
hapmaprs786204693
1000 genomesrs786204693
hgdprs786204693
ensemblrs786204693
gopubmedrs786204693
geneviewrs786204693
scholarrs786204693
googlers786204693
pharmgkbrs786204693
gwascentralrs786204693
openSNPrs786204693
23andMers786204693
23andMe allrs786204693
SNP Nexus

SNPshotrs786204693
SNPdbers786204693
MSV3drs786204693
GWAS Ctlgrs786204693
Max Magnitude0
ClinVar
Risk rs786204693(A;A)
Alt rs786204693(A;A)
Reference rs786204693(;)
Significance Probable-Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117176708dupA
CLNSRC
CLNACC RCV000169503.1,