SNP Report

Basic Info

Name	rs130146 dbSNP Ensembl
Location	chr22:48707465 - 48707465(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.39996
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000336769, ENST00000358295, ENST00000402357, ENST00000406880, ENST00000473898); non_coding_transcript_variant(ENST00000473898)
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)
FAM19A5	family with sequence similarity 19 (chemokine (C-C motif)-like), member A5	22q13.32	Mapped by Literature SNP

SNPs in LD with rs130146 (count: 0) View in gBrowse (chr22:48707465..48707465 )

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

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