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rs1064797340

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome7
Position107672192
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs1064797340
dbSNP (old)rs1064797340
ClinGenrs1064797340
ebirs1064797340
HLIrs1064797340
Exacrs1064797340
Gnomadrs1064797340
Varsomers1064797340
Maprs1064797340
PheGenIrs1064797340
Biobankrs1064797340
1000 genomesrs1064797340
hgdprs1064797340
ensemblrs1064797340
gopubmedrs1064797340
geneviewrs1064797340
scholarrs1064797340
googlers1064797340
pharmgkbrs1064797340
gwascentralrs1064797340
openSNPrs1064797340
23andMers1064797340
23andMe allrs1064797340
SNPshotrs1064797340
SNPdbers1064797340
MSV3drs1064797340
GWAS Ctlgrs1064797340
Max Magnitude0
ClinVar
Risk rs1064797340(T;T)
Alt rs1064797340(T;T)
Reference Rs1064797340(-;-)
Significance Probable-Pathogenic
Disease Pendred's syndrome not provided
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome not provided
Reversed 0
HGVS NC_000007.13:g.107312643dupT
CLNSRC
CLNACC RCV000169571.1, RCV000488403.1,