SNP Report

Basic Info

Name	rs1213392 dbSNP Ensembl
Location	chr10:35141357 - 35141357(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.420527
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000337656, ENST00000345491, ENST00000354759, ENST00000374721, ENST00000374726, ENST00000374728, ENST00000374734, ENST00000427847, ENST00000429130, ENST00000439705, ENST00000460270, ENST00000461968, ENST00000466251, ENST00000469949, ENST00000474362, ENST00000479070, ENST00000482633, ENST00000482646, ENST00000487132, ENST00000489321, ENST00000489388, ENST00000490460, ENST00000495960, ENST00000496019, ENST00000496626); NMD_transcript_variant(ENST00000490460, ENST00000495960); non_coding_transcript_variant(ENST00000461968, ENST00000466251, ENST00000482633, ENST00000482646, ENST00000489388, ENST00000496019, ENST00000496626)
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)
CREM	cAMP responsive element modulator	10p12.1-p11.1	1(0/1/0)

SNPs in LD with rs1213392 (count: 0) View in gBrowse (chr10:35141357..35141357 )

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

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