SNP Report

Basic Info

Name	rs9607632 dbSNP Ensembl
Location	chr22:39315720 - 39315720(1)
Variant Alleles	C/G
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.0227636
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000459859, ENST00000460589, ENST00000461967, ENST00000484615, ENST00000498462, ENST00000583861); intron_variant(ENST00000216146, ENST00000401609, ENST00000402527, ENST00000420536, ENST00000427905, ENST00000453303, ENST00000465618, ENST00000484358); NMD_transcript_variant(ENST00000420536); non_coding_transcript_variant(ENST00000465618, ENST00000484358); upstream_gene_variant(ENST00000386745, ENST00000386747, ENST00000464182, ENST00000467105, ENST00000471290, ENST00000473638, ENST00000481985)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 4)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
RPL3	ribosomal protein L3	22q13	Mapped by LD-proxy
SNORD83A	small nucleolar RNA, C/D box 83A	22q13.1	Mapped by LD-proxy
SNORD43	small nucleolar RNA, C/D box 43	22q13.1	Mapped by LD-proxy
SNORD83B	small nucleolar RNA, C/D box 83B	22q13.1	Mapped by LD-proxy

SNPs in LD with rs9607632 (count: 0) View in gBrowse (chr22:39315720..39315720 )

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

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