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rs199515730

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199515730(C;T)
Make rs199515730(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position145912475
GenePEX11B
is asnp
is mentioned by
dbSNPrs199515730
dbSNP (classic)rs199515730
ClinGenrs199515730
ebirs199515730
HLIrs199515730
Exacrs199515730
Gnomadrs199515730
Varsomers199515730
LitVarrs199515730
Maprs199515730
PheGenIrs199515730
Biobankrs199515730
1000 genomesrs199515730
hgdprs199515730
ensemblrs199515730
geneviewrs199515730
scholarrs199515730
googlers199515730
pharmgkbrs199515730
gwascentralrs199515730
openSNPrs199515730
23andMers199515730
23andMe allrs199515730
SNPshotrs199515730
SNPdbers199515730
MSV3drs199515730
GWAS Ctlgrs199515730
Max Magnitude0
ClinVar
Risk rs199515730(T;T)
Alt rs199515730(T;T)
Reference Rs199515730(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PEX11B
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.145522605C>T
CLNSRC
CLNACC RCV000478899.1,