SNP Report

Basic Info

Name	rs17691328 dbSNP Ensembl
Location	chrCHR_HSCHR17_2_CTG5:45889745 - 45889745(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.0866613
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000579244, ENST00000579599, ENST00000634876); non_coding_transcript_variant(ENST00000579244, ENST00000579599, ENST00000634876, ENST00000628274, ENST00000629948, ENST00000628274, ENST00000629948, 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: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
MAPT-AS1	MAPT antisense RNA 1	17q21.31	Mapped by Literature SNP

SNPs in LD with rs17691328 (count: 0) View in gBrowse (chrCHR_HSCHR17_2_CTG5:45889745..45889745 )

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

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