SNP Report

Basic Info

Name	rs1295101 dbSNP Ensembl
Location	chr1:5996108 - 5996108(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.401757
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000378092, ENST00000378097, ENST00000378111, ENST00000445501, ENST00000478098, ENST00000493807); non_coding_transcript_variant(ENST00000478098, ENST00000493807); upstream_gene_variant(ENST00000378156, ENST00000378169, ENST00000478423, ENST00000489180, ENST00000622020)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
NPHP4	nephronophthisis 4	1p36	1(1/0/0)
KCNAB2	potassium channel, voltage gated subfamily A regulatory beta subunit 2	1p36.3	Mapped by LD-proxy

SNPs in LD with rs1295101 (count: 0) View in gBrowse (chr1:5996108..5996108 )

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

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