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rs786204450

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204450(-;-)
Make rs786204450(-;C)
Make rs786204450(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107698044
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs786204450
ebirs786204450
HLIrs786204450
Exacrs786204450
Varsomers786204450
Maprs786204450
PheGenIrs786204450
hapmaprs786204450
1000 genomesrs786204450
hgdprs786204450
ensemblrs786204450
gopubmedrs786204450
geneviewrs786204450
scholarrs786204450
googlers786204450
pharmgkbrs786204450
gwascentralrs786204450
openSNPrs786204450
23andMers786204450
23andMe allrs786204450
SNP Nexus

SNPshotrs786204450
SNPdbers786204450
MSV3drs786204450
GWAS Ctlgrs786204450
Max Magnitude0
ClinVar
Risk rs786204450(C;C)
Alt rs786204450(C;C)
Reference rs786204450(;)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107338489dupC
CLNSRC
CLNACC RCV000169076.1,