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rs376710410

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs376710410(A;C)
Make rs376710410(C;C)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position33065551
GeneGLB1
is asnp
is mentioned by
dbSNPrs376710410
dbSNP (classic)rs376710410
ClinGenrs376710410
ebirs376710410
HLIrs376710410
Exacrs376710410
Gnomadrs376710410
Varsomers376710410
LitVarrs376710410
Maprs376710410
PheGenIrs376710410
Biobankrs376710410
1000 genomesrs376710410
hgdprs376710410
ensemblrs376710410
geneviewrs376710410
scholarrs376710410
googlers376710410
pharmgkbrs376710410
gwascentralrs376710410
openSNPrs376710410
23andMers376710410
SNPshotrs376710410
SNPdbers376710410
MSV3drs376710410
GWAS Ctlgrs376710410
Max Magnitude0
ClinVar
Risk rs376710410(C;C)
Alt rs376710410(C;C)
Reference Rs376710410(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TMPPE GLB1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.33107043A>C
CLNSRC
CLNACC RCV000256106.1,