SNP Report

Basic Info

Name	rs885639 dbSNP Ensembl
Location	chrCHR_HSCHR17_2_CTG5:45862866 - 45862866(1)
Variant Alleles	T/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.122804
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000329196); intron_variant(ENST00000579244, ENST00000579599, ENST00000634876); non_coding_transcript_variant(ENST00000579244, ENST00000579599, ENST00000634876, ENST00000610319, ENST00000628274, ENST00000629948, ENST00000628274, ENST00000629948, ENST00000621383, ENST00000632082, ENST00000633517, ENST00000632082, ENST00000633517)
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)
MAPT-AS1	MAPT antisense RNA 1	17q21.31	Mapped by Literature SNP
SPPL2C	signal peptide peptidase like 2C	17q21.31	Mapped by Literature SNP

SNPs in LD with rs885639 (count: 0) View in gBrowse (chrCHR_HSCHR17_2_CTG5:45862866..45862866 )

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

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