SNP Report

Basic Info

Name	rs10849949 dbSNP Ensembl
Location	chr12:111455733 - 111455733(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.464457
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000550844); downstream_gene_variant(ENST00000341259, ENST00000468920, ENST00000550889, ENST00000551551); intron_variant(ENST00000377617, ENST00000389153, ENST00000389154, ENST00000475132, ENST00000483311, ENST00000535949, ENST00000542287, ENST00000550104, ENST00000608853, ENST00000616825); NMD_transcript_variant(ENST00000483311); non_coding_transcript_exon_variant(ENST00000482777); non_coding_transcript_variant(ENST00000482777); upstream_gene_variant(ENST00000484991)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
SH2B3	SH2B adaptor protein 3	12q24.12	Mapped by Literature SNP
ATXN2	ataxin 2	12q23-q24.1	Mapped by LD-proxy

SNPs in LD with rs10849949 (count: 0) View in gBrowse (chr12:111455733..111455733 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)