SNP Report

Basic Info

Name	rs137919 dbSNP Ensembl
Location	chr22:50061535 - 50061535(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.282947
Functional Annotation	3_prime_UTR_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000311597, ENST00000395876); non_coding_transcript_exon_variant(ENST00000483836); non_coding_transcript_variant(ENST00000483836); upstream_gene_variant(ENST00000433387)
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)
MLC1	megalencephalic leukoencephalopathy with subcortical cysts 1	22q13.33	5(1/4/0)
TTLL8	tubulin tyrosine ligase-like family member 8	22q13.33	Mapped by LD-proxy

SNPs in LD with rs137919 (count: 0) View in gBrowse (chr22:50061535..50061535 )

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

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