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SNP Report
Name | rs6937334 dbSNP Ensembl | ||
---|---|---|---|
Location | chr6:17935773 - 17935773(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.283347 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000259711, ENST00000378814, ENST00000378826, ENST00000378843, ENST00000505588, ENST00000507576, ENST00000636847); non_coding_transcript_variant(ENST00000505588, ENST00000507576) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |