SNP Report

Basic Info

Name	rs60035268 dbSNP Ensembl
Location	chr4:1093699 - 1093699(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.0521166
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; stop_gained.
Consequence to Transcript	downstream_gene_variant(ENST00000454487); intron_variant(ENST00000382968, ENST00000433731, ENST00000506730, ENST00000508428, ENST00000510715, ENST00000511620, ENST00000512552); NMD_transcript_variant(ENST00000506730, ENST00000508428, ENST00000510715, ENST00000511620); non_coding_transcript_variant(ENST00000512552); stop_gained(ENST00000333673)
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	G/A		GERP=1.03 GERP=1.03	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)
RNF212	ring finger protein 212	4p16.3	1(0/0/1)

SNPs in LD with rs60035268 (count: 0) View in gBrowse (chr4:1093699..1093699 )

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

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