SNP Report

Basic Info

Name	rs201826382 dbSNP Ensembl
Location	chr19:8956561 - 8956561(1)
Variant Alleles	T/G
Ancestral Allele	T
Minor Allele Frequence	0.0
Functional Annotation	missense_variant. Polyphen Annotation: unknown(ENST00000397910)
Consequence to Transcript	missense_variant(ENST00000397910)
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	T/G		7 in BPI, 3 in Well 7 in BPI, 3 in Well	Top 30 Amish-specific putative damaging exonic missense vari...... Top 30 Amish-specific putative damaging exonic missense variants by prevalence in affected individuals. More...	Trend

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
MUC16	mucin 16, cell surface associated	19p13.2	1(0/0/1)

SNPs in LD with rs201826382 (count: 0) View in gBrowse (chr19:8956561..8956561 )

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

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