SNP Report

Basic Info

Name	rs995472 dbSNP Ensembl
Location	chr2:204729922 - 204729922(1)
Variant Alleles	T/A
Ancestral Allele	T
Minor Allele	A
Minor Allele Frequence	0.179513
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000349953, ENST00000351153, ENST00000358768, ENST00000406610, ENST00000415947, ENST00000462231); NMD_transcript_variant(ENST00000415947)
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)
PARD3B	par-3 family cell polarity regulator beta	2q33.3	Mapped by Literature SNP

SNPs in LD with rs995472 (count: 0) View in gBrowse (chr2:204729922..204729922 )

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

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