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)