SNP Report

Basic Info

Name	rs6003579 dbSNP Ensembl
Location	chr22:23231680 - 23231680(1)
Variant Alleles	G/C
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.348642
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000305877, ENST00000359540, ENST00000398512, ENST00000463770, ENST00000479188, ENST00000487679); non_coding_transcript_variant(ENST00000463770, ENST00000479188, ENST00000487679)
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)
BCR	breakpoint cluster region	22q11	2(1/1/0)

SNPs in LD with rs6003579 (count: 0) View in gBrowse (chr22:23231680..23231680 )

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

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