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SNP Report
Name | rs2071436 dbSNP Ensembl | ||
---|---|---|---|
Location | chr22:23199301 - 23199301(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.226438 | ||
Functional Annotation | intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000305877, ENST00000359540, ENST00000398512, ENST00000463770, ENST00000479188); non_coding_transcript_exon_variant(ENST00000487679); non_coding_transcript_variant(ENST00000463770, ENST00000479188, ENST00000487679) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |