Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.32 (C)
Location

Chromosome 22:37258503 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs34912150, rs59821819

This variation has 8 HGVS names - click the plus to show

22:g.37258503T>C
ENST00000447071.1:c.-193+1258T>C
ENST00000397147.4:c.32+1258T>C
ENST00000330602.2:n.349+7632A>G
ENST00000248899.6:c.32+1258T>C
ENST00000431290.1:n.289-4218A>G
LRG_159:g.6474T>C
LRG_159t1.1:c.32+1258T>C

This variation has assays on 11 chips - click the plus to show

Variation displays