SNP Report

Basic Info

Name	rs1010035 dbSNP Ensembl
Location	chr22:34703486 - 34703486(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.335863
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000423712); non_coding_transcript_variant(ENST00000423712)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs1010035 (count: 0) View in gBrowse (chr22:34703486..34703486 )

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

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