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rs748510210

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs748510210(A;A)
Make rs748510210(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position201628075
GeneTMEM237
is asnp
is mentioned by
dbSNPrs748510210
ebirs748510210
HLIrs748510210
Exacrs748510210
Varsomers748510210
Maprs748510210
PheGenIrs748510210
hapmaprs748510210
1000 genomesrs748510210
hgdprs748510210
ensemblrs748510210
gopubmedrs748510210
geneviewrs748510210
scholarrs748510210
googlers748510210
pharmgkbrs748510210
gwascentralrs748510210
openSNPrs748510210
23andMers748510210
23andMe allrs748510210
SNP Nexus

SNPshotrs748510210
SNPdbers748510210
MSV3drs748510210
GWAS Ctlgrs748510210
Max Magnitude0
ClinVar
Risk rs748510210(A;A)
Alt rs748510210(A;A)
Reference rs748510210(C;C)
Significance Pathogenic
Disease Joubert syndrome 14
Variation info
Gene TMEM237
CLNDBN Joubert syndrome 14
Reversed 0
HGVS NC_000002.11:g.202492798C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000024183.4,