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rs201636911

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201636911(A;A)
Make rs201636911(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107661783
GeneSLC26A4, SLC26A4-AS1
is asnp
is mentioned by
dbSNPrs201636911
dbSNP (old)rs201636911
ClinGenrs201636911
ebirs201636911
HLIrs201636911
Exacrs201636911
Gnomadrs201636911
Varsomers201636911
Maprs201636911
PheGenIrs201636911
Biobankrs201636911
1000 genomesrs201636911
hgdprs201636911
ensemblrs201636911
gopubmedrs201636911
geneviewrs201636911
scholarrs201636911
googlers201636911
pharmgkbrs201636911
gwascentralrs201636911
openSNPrs201636911
23andMers201636911
23andMe allrs201636911
SNPshotrs201636911
SNPdbers201636911
MSV3drs201636911
GWAS Ctlgrs201636911
Max Magnitude0
ClinVar
Risk rs201636911(A;A) rs201636911(T;T)
Alt rs201636911(A;A) rs201636911(T;T)
Reference Rs201636911(G;G)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4-AS1 SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107302228G>T
CLNSRC
CLNACC RCV000409402.1,