SNP Report

Basic Info

Name	rs370175066 dbSNP Ensembl
Location	chr16:14252476 - 14252476(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele Frequence	0.0
Functional Annotation	missense_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant. Polyphen Annotation: benign(ENST00000318282, ENST00000574045); probably damaging(ENST00000571589) SIFT Annotation: deleterious(ENST00000318282, ENST00000574045, ENST00000571589)
Consequence to Transcript	missense_variant(ENST00000318282, ENST00000574045, ENST00000571589); non_coding_transcript_exon_variant(ENST00000572588); non_coding_transcript_variant(ENST00000572588)
No. of Studies	1 (Positive: 0; Negative: 0; Trend: 1)
Source	Literature
Overlap with SZ?	NO
Overlap with MDD?	NO

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result Category
Georgi, B., 2014	C/T		GERP=5.84 GERP=5.84	Putative damaging exonic variants found in the five linkage ...... Putative damaging exonic variants found in the five linkage regions. More...	Trend

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
MKL2	MKL/myocardin-like 2	16p13.12	1(0/0/1)

SNPs in LD with rs370175066 (count: 0) View in gBrowse (chr16:14252476..14252476 )

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

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