SNP Report

Basic Info

Name	rs13003991 dbSNP Ensembl
Location	chr2:65545822 - 65545822(1)
Variant Alleles	C/G
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.388379
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000377977, ENST00000606978); non_coding_transcript_variant(ENST00000377977, ENST00000606978); upstream_gene_variant(ENST00000492123)
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)
RN7SL635P	RNA, 7SL, cytoplasmic 635, pseudogene	2p14	Mapped by LD-proxy

SNPs in LD with rs13003991 (count: 0) View in gBrowse (chr2:65545822..65545822 )

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

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