SNP Report

Basic Info

Name	rs17691610 dbSNP Ensembl
Location	chrCHR_HSCHR17_2_CTG5:45904924 - 45904924(1)
Variant Alleles	G/T
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.0860623
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000579244, ENST00000579599, ENST00000634876); non_coding_transcript_variant(ENST00000579244, ENST00000579599, ENST00000634876); upstream_gene_variant(ENST00000262410, ENST00000334239, ENST00000340799, ENST00000344290, ENST00000351559, ENST00000446361, ENST00000535772, ENST00000570299, ENST00000571311, ENST00000624111, ENST00000628274, ENST00000629948, ENST00000628274, ENST00000629948, ENST00000625688, ENST00000626571, ENST00000626958, ENST00000627067, ENST00000628393, ENST00000632082, ENST00000633517, ENST00000632082, ENST00000633517, ENST00000612872, ENST00000618029, ENST00000618825, ENST00000620070, ENST00000620818, ENST00000622106, ENST00000632975, ENST00000633047, ENST00000633415, ENST00000633806)
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
MAPT	microtubule-associated protein tau	17q21	Mapped by Literature SNP

SNPs in LD with rs17691610 (count: 0) View in gBrowse (chrCHR_HSCHR17_2_CTG5:45904924..45904924 )

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

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