SNP Report

Basic Info

Name	rs6222 dbSNP Ensembl
Location	chr12:102396123 - 102396123(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.0201677
Functional Annotation	3_prime_UTR_variant; intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000337514, ENST00000456098); intron_variant(ENST00000635615); non_coding_transcript_exon_variant(ENST00000626826); non_coding_transcript_variant(ENST00000626826, ENST00000635615)
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)
IGF1	insulin-like growth factor 1 (somatomedin C)	12q23.2	1(1/0/0)

SNPs in LD with rs6222 (count: 0) View in gBrowse (chr12:102396123..102396123 )

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

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