SNP Report

Basic Info

Name	rs916896 dbSNP Ensembl
Location	chrCHR_HSCHR17_2_CTG5:46033040 - 46033040(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.314896
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000570299); intron_variant(ENST00000262410, ENST00000334239, ENST00000340799, ENST00000344290, ENST00000351559, ENST00000415613, ENST00000420682, ENST00000431008, ENST00000446361, ENST00000535772, ENST00000571987, ENST00000574436, ENST00000576518); non_coding_transcript_variant(ENST00000576518, ENST00000627067, ENST00000613360, ENST00000620981, ENST00000621329, ENST00000622728, ENST00000626571, ENST00000626880, ENST00000627711, ENST00000628393, ENST00000629368, ENST00000626880, ENST00000632975, ENST00000612872, ENST00000618029, ENST00000618825, ENST00000620070, ENST00000620818, ENST00000622106, ENST00000631447, ENST00000632122, ENST00000632500, ENST00000633047, ENST00000633054, ENST00000633801, ENST00000634049)
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	microtubule-associated protein tau	17q21	Mapped by Literature SNP

SNPs in LD with rs916896 (count: 0) View in gBrowse (chrCHR_HSCHR17_2_CTG5:46033040..46033040 )

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

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