SNP Report

Basic Info

Name	rs11636157 dbSNP Ensembl
Location	chr15:61550358 - 61550358(1)
Variant Alleles	A/C
Ancestral Allele	A
Minor Allele	C
Minor Allele Frequence	0.48103
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000559783); non_coding_transcript_variant(ENST00000559783)
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 rs11636157 (count: 0) View in gBrowse (chr15:61550358..61550358 )

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

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