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SNP Report
Name | rs3753299 dbSNP Ensembl | ||
---|---|---|---|
Location | chr1:169207781 - 169207781(1) | ||
Variant Alleles | G/T | ||
Ancestral Allele | G | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.196685 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000367811, ENST00000472647, ENST00000483228, ENST00000493481, ENST00000525440); NMD_transcript_variant(ENST00000525440); non_coding_transcript_variant(ENST00000483228, ENST00000493481) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |