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rs754369980

From SNPedia

Orientationplus
Stabilizedplus
Make rs754369980(-;-)
Make rs754369980(-;C)
Make rs754369980(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position30965995
GeneSETD1A
is asnp
is mentioned by
dbSNPrs754369980
dbSNP (old)rs754369980
ClinGenrs754369980
ebirs754369980
HLIrs754369980
Exacrs754369980
Gnomadrs754369980
Varsomers754369980
Maprs754369980
PheGenIrs754369980
Biobankrs754369980
1000 genomesrs754369980
hgdprs754369980
ensemblrs754369980
gopubmedrs754369980
geneviewrs754369980
scholarrs754369980
googlers754369980
pharmgkbrs754369980
gwascentralrs754369980
openSNPrs754369980
23andMers754369980
23andMe allrs754369980
SNP Nexus

SNPshotrs754369980
SNPdbers754369980
MSV3drs754369980
GWAS Ctlgrs754369980
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 16:30977316_G/GC and also as p.G705fs