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rs762131795

From SNPedia

Orientationplus
Stabilizedplus
Make rs762131795(-;-)
Make rs762131795(-;AG)
Make rs762131795(AG;AG)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position30966085
GeneSETD1A
is asnp
is mentioned by
dbSNPrs762131795
dbSNP (old)rs762131795
ClinGenrs762131795
ebirs762131795
HLIrs762131795
Exacrs762131795
Gnomadrs762131795
Varsomers762131795
Maprs762131795
PheGenIrs762131795
Biobankrs762131795
1000 genomesrs762131795
hgdprs762131795
ensemblrs762131795
gopubmedrs762131795
geneviewrs762131795
scholarrs762131795
googlers762131795
pharmgkbrs762131795
gwascentralrs762131795
openSNPrs762131795
23andMers762131795
23andMe allrs762131795
SNP Nexus

SNPshotrs762131795
SNPdbers762131795
MSV3drs762131795
GWAS Ctlgrs762131795
Max Magnitude
[PMID 26974950] Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

referred to in the cited paper as 16:30977405_CAG/C and also as p.Q735fs