Have questions? Visit https://www.reddit.com/r/SNPedia

rs2019877

From SNPedia

Orientationplus
Stabilizedplus
Make rs2019877(C;C)
Make rs2019877(C;T)
Make rs2019877(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position73763821
GeneLINC00469
is asnp
is mentioned by
dbSNPrs2019877
dbSNP (classic)rs2019877
ClinGenrs2019877
ebirs2019877
HLIrs2019877
Exacrs2019877
Gnomadrs2019877
Varsomers2019877
LitVarrs2019877
Maprs2019877
PheGenIrs2019877
Biobankrs2019877
1000 genomesrs2019877
hgdprs2019877
ensemblrs2019877
geneviewrs2019877
scholarrs2019877
googlers2019877
pharmgkbrs2019877
gwascentralrs2019877
openSNPrs2019877
23andMers2019877
SNPshotrs2019877
SNPdbers2019877
MSV3drs2019877
GWAS Ctlgrs2019877
GMAF0.3829
Max Magnitude0
? (C;C) (C;T) (T;T) 28


OMIM277470
DescPONTOCEREBELLAR HYPOPLASIA TYPE 2A; PCH2A
Variant
Relatedalso