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SNP Report
Name | rs7986477 dbSNP Ensembl | ||
---|---|---|---|
Location | chr13:98847097 - 98847097(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.253195 | ||
Functional Annotation | 5_prime_UTR_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | 5_prime_UTR_variant(ENST00000340449); intron_variant(ENST00000339416, ENST00000376460, ENST00000442173, ENST00000448493, ENST00000449796, ENST00000450257, ENST00000472874, ENST00000630992); NMD_transcript_variant(ENST00000339416, ENST00000630992); non_coding_transcript_variant(ENST00000472874) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |