SNP Report

Basic Info

Name	rs7127529 dbSNP Ensembl
Location	chr11:46560522 - 46560522(1)
Variant Alleles	A/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.203275
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000314845, ENST00000458649, ENST00000526606, ENST00000528950, ENST00000531542, ENST00000533727, ENST00000534300); non_coding_transcript_variant(ENST00000531542)
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)
AMBRA1	autophagy/beclin-1 regulator 1	11p11.2	Mapped by LD-proxy

SNPs in LD with rs7127529 (count: 0) View in gBrowse (chr11:46560522..46560522 )

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

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