SNP Report

Basic Info

Name	rs2635197 dbSNP Ensembl
Location	chr4:117649151 - 117649151(1)
Variant Alleles	C/G
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.140375
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000422145, ENST00000600624, ENST00000615833, ENST00000626258); non_coding_transcript_variant(ENST00000422145, ENST00000600624, ENST00000615833, ENST00000626258)
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 rs2635197 (count: 0) View in gBrowse (chr4:117649151..117649151 )

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

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