SNP Report

Basic Info

Name	rs9617070 dbSNP Ensembl
Location	chr22:50096153 - 50096153(1)
Variant Alleles	C/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.247404
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000262794, ENST00000395854, ENST00000395858, ENST00000419054, ENST00000475190, ENST00000540615, ENST00000545383); NMD_transcript_variant(ENST00000395854, ENST00000419054); non_coding_transcript_exon_variant(ENST00000623740); non_coding_transcript_variant(ENST00000475190, ENST00000623740)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
MOV10L1	Mov10 RISC complex RNA helicase like 1	22q13.33	1(0/1/0)

SNPs in LD with rs9617070 (count: 0) View in gBrowse (chr22:50096153..50096153 )

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

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