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rs61744449

From SNPedia

Orientationplus
Make rs61744449(C;C)
Make rs61744449(C;G)
Make rs61744449(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position30969641
GeneSETD1A
is asnp
is mentioned by
dbSNPrs61744449
ebirs61744449
HLIrs61744449
Exacrs61744449
Varsomers61744449
Maprs61744449
PheGenIrs61744449
hapmaprs61744449
1000 genomesrs61744449
hgdprs61744449
ensemblrs61744449
gopubmedrs61744449
geneviewrs61744449
scholarrs61744449
googlers61744449
pharmgkbrs61744449
gwascentralrs61744449
openSNPrs61744449
23andMers61744449
23andMe allrs61744449
SNP Nexus

SNPshotrs61744449
SNPdbers61744449
MSV3drs61744449
GWAS Ctlgrs61744449
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 16:30980962_C/T and also as p.R990X