Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.22 (T)
Location

Chromosome 7:155254145 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS045644

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3808333

This variation has 2 HGVS names - click the plus to show

7:g.155254145T>C
ENST00000297375.4:c.686-921T>C

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5

Variation displays