SNP Report

Basic Info
Name rs3135737 dbSNP Ensembl
Location chr10:121553445 - 121553445(1)
Variant Alleles A/G
Ancestral Allele A
Minor Allele G
Minor Allele Frequence 0.117612
Functional Annotation intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000336553, ENST00000346997, ENST00000351936, ENST00000356226, ENST00000357555, ENST00000358487, ENST00000359354, ENST00000360144, ENST00000369056, ENST00000369058, ENST00000369059, ENST00000369060, ENST00000369061, ENST00000457416, ENST00000490349, ENST00000604236, ENST00000613048); NMD_transcript_variant(ENST00000604236); non_coding_transcript_variant(ENST00000490349)
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)
FGFR2 fibroblast growth factor receptor 2 10q25.3-q26 2(1/1/0)

SNPs in LD with rs3135737 (count: 0) View in gBrowse (chr10:121553445..121553445 )

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

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