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rs374963432

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs374963432(G;T)
Make rs374963432(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position150941647
GeneCLRN1
is asnp
is mentioned by
dbSNPrs374963432
ebirs374963432
HLIrs374963432
Exacrs374963432
Varsomers374963432
Maprs374963432
PheGenIrs374963432
hapmaprs374963432
1000 genomesrs374963432
hgdprs374963432
ensemblrs374963432
gopubmedrs374963432
geneviewrs374963432
scholarrs374963432
googlers374963432
pharmgkbrs374963432
gwascentralrs374963432
openSNPrs374963432
23andMers374963432
23andMe allrs374963432
SNP Nexus

SNPshotrs374963432
SNPdbers374963432
MSV3drs374963432
GWAS Ctlgrs374963432
Max Magnitude0
ClinVar
Risk rs374963432(T;T)
Alt rs374963432(T;T)
Reference rs374963432(G;G)
Significance Other
Disease Usher syndrome
Variation info
Gene CLRN1
CLNDBN Usher syndrome, type 3A
Reversed 0
HGVS NC_000003.11:g.150659434G>T
CLNSRC ClinVar
CLNACC RCV000041436.4,