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SNP Report
Name | rs10216219 dbSNP Ensembl | ||
---|---|---|---|
Location | chr7:148781628 - 148781628(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.208267 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000325222, ENST00000409469, ENST00000602748, ENST00000617797) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |